http://identifiers.org/exac.variant/14-24839234-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839234
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839234
    reference: chr 14
allele count: 2
allele frequency: 1.748985588358752e-5
allele num: 114352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.629C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.594C>A
  hgvsp: ENST00000422617.3:c.594C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.420C>A
  hgvsp: ENST00000553879.1:c.420C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.819C>A
  hgvsp: ENST00000413692.2:c.819C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452352
  ensembl transcript: ENST00000557674
  gene symbol: NFATC4
  hgvsc: ENST00000557674.1:c.561C>A
  hgvsp: ENST00000557674.1:c.561C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.420C>A
  hgvsp: ENST00000554344.1:c.420C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.669C>A
  hgvsp: ENST00000555590.1:c.669C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.630C>A
  hgvsp: ENST00000250373.4:c.630C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+358C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.594C>A
  hgvsp: ENST00000555453.1:c.594C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.726C>A
  hgvsp: ENST00000556279.1:c.726C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.630C>A
  hgvsp: ENST00000554050.1:c.630C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.830C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.819C>A
  hgvsp: ENST00000554591.1:c.819C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.669C>A
  hgvsp: ENST00000554966.1:c.669C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.726C>A
  hgvsp: ENST00000539237.2:c.726C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.420C>A
  hgvsp: ENST00000557451.1:c.420C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.726C>A
  hgvsp: ENST00000553469.1:c.726C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.669C>A
  hgvsp: ENST00000424781.2:c.669C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly273Gly
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS

14-24839245-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839245
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839245
    reference: chr 14
allele count: 1
allele frequency: 8.787655102112552e-6
allele num: 113796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.680C>T
  hgvsp: ENSP00000450644.1:p.Pro227Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.641C>T
  hgvsp: ENSP00000250373.4:p.Pro214Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+369C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.830C>T
  hgvsp: ENSP00000452039.1:p.Pro277Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.934C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.605C>T
  hgvsp: ENSP00000396788.3:p.Pro202Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.680C>T
  hgvsp: ENSP00000451224.1:p.Pro227Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.737C>T
  hgvsp: ENSP00000439350.2:p.Pro246Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.680C>T
  hgvsp: ENSP00000388668.2:p.Pro227Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.640C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.641C>T
  hgvsp: ENSP00000450590.1:p.Pro214Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.431C>T
  hgvsp: ENSP00000450469.1:p.Pro144Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.431C>T
  hgvsp: ENSP00000450733.1:p.Pro144Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.641C>T
  hgvsp: ENSP00000451151.1:p.Pro214Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.841C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.605C>T
  hgvsp: ENSP00000451454.1:p.Pro202Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.431C>T
  hgvsp: ENSP00000452349.1:p.Pro144Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452352
  ensembl transcript: ENST00000557674
  gene symbol: NFATC4
  hgvsc: ENST00000557674.1:c.572C>T
  hgvsp: ENSP00000452352.1:p.Pro191Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.605C>T
  hgvsp: ENSP00000450686.1:p.Pro202Leu
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro277Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

14-24839246-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839246
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839246
    reference: chr 14
allele count: 1
allele frequency: 8.789354334030623e-6
allele num: 113774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.432G>A
  hgvsp: ENST00000554344.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.681G>A
  hgvsp: ENST00000554966.1:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+370G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.606G>A
  hgvsp: ENST00000556169.1:c.606G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.432G>A
  hgvsp: ENST00000557451.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452352
  ensembl transcript: ENST00000557674
  gene symbol: NFATC4
  hgvsc: ENST00000557674.1:c.573G>A
  hgvsp: ENST00000557674.1:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.642G>A
  hgvsp: ENST00000554050.1:c.642G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.681G>A
  hgvsp: ENST00000555590.1:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.432G>A
  hgvsp: ENST00000553879.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.642G>A
  hgvsp: ENST00000250373.4:c.642G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+370G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.831G>A
  hgvsp: ENST00000554591.1:c.831G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.738G>A
  hgvsp: ENST00000539237.2:c.738G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.606G>A
  hgvsp: ENST00000555453.1:c.606G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.681G>A
  hgvsp: ENST00000424781.2:c.681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.842G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.738G>A
  hgvsp: ENST00000556279.1:c.738G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.642G>A
  hgvsp: ENST00000553708.1:c.642G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.432G>A
  hgvsp: ENST00000554661.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro277Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

14-24839246-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839246
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839246
    reference: chr 14
allele count: 2
allele frequency: 1.757870866806125e-5
allele num: 113774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.738G>T
  hgvsp: ENST00000556279.1:c.738G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.681G>T
  hgvsp: ENST00000424781.2:c.681G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.831G>T
  hgvsp: ENST00000413692.2:c.831G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.681G>T
  hgvsp: ENST00000555590.1:c.681G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+370G>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.681G>T
  hgvsp: ENST00000554966.1:c.681G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.831G>T
  hgvsp: ENST00000554591.1:c.831G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.432G>T
  hgvsp: ENST00000553879.1:c.432G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.842G>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.606G>T
  hgvsp: ENST00000422617.3:c.606G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+370G>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.935G>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452352
  ensembl transcript: ENST00000557674
  gene symbol: NFATC4
  hgvsc: ENST00000557674.1:c.573G>T
  hgvsp: ENST00000557674.1:c.573G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.432G>T
  hgvsp: ENST00000557451.1:c.432G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.432G>T
  hgvsp: ENST00000554344.1:c.432G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.738G>T
  hgvsp: ENST00000553469.1:c.738G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.642G>T
  hgvsp: ENST00000553708.1:c.642G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.606G>T
  hgvsp: ENST00000556169.1:c.606G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.641G>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.642G>T
  hgvsp: ENST00000250373.4:c.642G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro277Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

14-24839249-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839249
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839249
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 113808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.766G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.435G>A
  hgvsp: ENST00000553879.1:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.834G>A
  hgvsp: ENST00000554591.1:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.609G>A
  hgvsp: ENST00000556169.1:c.609G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.435G>A
  hgvsp: ENST00000557451.1:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.741G>A
  hgvsp: ENST00000556279.1:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.684G>A
  hgvsp: ENST00000424781.2:c.684G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.834G>A
  hgvsp: ENST00000413692.2:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.741G>A
  hgvsp: ENST00000553469.1:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.609G>A
  hgvsp: ENST00000555453.1:c.609G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.644G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.645G>A
  hgvsp: ENST00000554050.1:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.741G>A
  hgvsp: ENST00000539237.2:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.938G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.645G>A
  hgvsp: ENST00000250373.4:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.435G>A
  hgvsp: ENST00000554661.1:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.684G>A
  hgvsp: ENST00000555590.1:c.684G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.435G>A
  hgvsp: ENST00000554344.1:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.845G>A
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu278Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

14-24839260-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839260
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839260
    reference: chr 14
allele count: 1
allele frequency: 8.818653215280963e-6
allele num: 113396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.777G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.446G>C
  hgvsp: ENSP00000450733.1:p.Arg149Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.752G>C
  hgvsp: ENSP00000451502.1:p.Arg251Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.695G>C
  hgvsp: ENSP00000388668.2:p.Arg232Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.845G>C
  hgvsp: ENSP00000388910.2:p.Arg282Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.656G>C
  hgvsp: ENSP00000451151.1:p.Arg219Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.446G>C
  hgvsp: ENSP00000452349.1:p.Arg149Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.695G>C
  hgvsp: ENSP00000451224.1:p.Arg232Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.446G>C
  hgvsp: ENSP00000450469.1:p.Arg149Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.695G>C
  hgvsp: ENSP00000450644.1:p.Arg232Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.845G>C
  hgvsp: ENSP00000452039.1:p.Arg282Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.856G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.620G>C
  hgvsp: ENSP00000451454.1:p.Arg207Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452352
  ensembl transcript: ENST00000557674
  gene symbol: NFATC4
  hgvsc: ENST00000557674.1:c.587G>C
  hgvsp: ENSP00000452352.1:p.Arg196Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.752G>C
  hgvsp: ENSP00000452270.1:p.Arg251Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.655G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+384G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.620G>C
  hgvsp: ENSP00000450686.1:p.Arg207Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+384G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.656G>C
  hgvsp: ENSP00000250373.4:p.Arg219Pro
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg282Pro
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

14-24839261-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839261
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839261
    reference: chr 14
allele count: 1
allele frequency: 8.813989564236357e-6
allele num: 113456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.950G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.447G>A
  hgvsp: ENST00000554344.1:c.447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.621G>A
  hgvsp: ENST00000422617.3:c.621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+385G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452352
  ensembl transcript: ENST00000557674
  gene symbol: NFATC4
  hgvsc: ENST00000557674.1:c.588G>A
  hgvsp: ENST00000557674.1:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.696G>A
  hgvsp: ENST00000424781.2:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.696G>A
  hgvsp: ENST00000554966.1:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.656G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.621G>A
  hgvsp: ENST00000555453.1:c.621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+385G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.846G>A
  hgvsp: ENST00000554591.1:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.657G>A
  hgvsp: ENST00000554050.1:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.621G>A
  hgvsp: ENST00000556169.1:c.621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.447G>A
  hgvsp: ENST00000553879.1:c.447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.753G>A
  hgvsp: ENST00000539237.2:c.753G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.753G>A
  hgvsp: ENST00000556279.1:c.753G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.857G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.657G>A
  hgvsp: ENST00000250373.4:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.657G>A
  hgvsp: ENST00000553708.1:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.696G>A
  hgvsp: ENST00000555590.1:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg282Arg
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-24839264-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839264
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839264
    reference: chr 14
allele count: 1
allele frequency: 8.8281512085739e-6
allele num: 113274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.756C>A
  hgvsp: ENST00000539237.2:c.756C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.699C>A
  hgvsp: ENST00000555590.1:c.699C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.849C>A
  hgvsp: ENST00000413692.2:c.849C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.756C>A
  hgvsp: ENST00000556279.1:c.756C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.450C>A
  hgvsp: ENST00000554344.1:c.450C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.699C>A
  hgvsp: ENST00000554966.1:c.699C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.849C>A
  hgvsp: ENST00000554591.1:c.849C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.699C>A
  hgvsp: ENST00000424781.2:c.699C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.450C>A
  hgvsp: ENST00000553879.1:c.450C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.660C>A
  hgvsp: ENST00000554050.1:c.660C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.660C>A
  hgvsp: ENST00000250373.4:c.660C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.624C>A
  hgvsp: ENST00000556169.1:c.624C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.450C>A
  hgvsp: ENST00000557451.1:c.450C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.450C>A
  hgvsp: ENST00000554661.1:c.450C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.953C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.660C>A
  hgvsp: ENST00000553708.1:c.660C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.860C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+388C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.756C>A
  hgvsp: ENST00000553469.1:c.756C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala283Ala
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

14-24839264-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839264
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839264
    reference: chr 14
allele count: 1
allele frequency: 8.8281512085739e-6
allele num: 113274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.624C>T
  hgvsp: ENST00000422617.3:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.699C>T
  hgvsp: ENST00000554966.1:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.450C>T
  hgvsp: ENST00000557451.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.781C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.450C>T
  hgvsp: ENST00000554661.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.699C>T
  hgvsp: ENST00000555590.1:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.756C>T
  hgvsp: ENST00000556279.1:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+388C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.450C>T
  hgvsp: ENST00000553879.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.450C>T
  hgvsp: ENST00000554344.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.953C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.659C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.756C>T
  hgvsp: ENST00000553469.1:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.624C>T
  hgvsp: ENST00000555453.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.756C>T
  hgvsp: ENST00000539237.2:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.660C>T
  hgvsp: ENST00000553708.1:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.660C>T
  hgvsp: ENST00000554050.1:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.849C>T
  hgvsp: ENST00000554591.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.660C>T
  hgvsp: ENST00000250373.4:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala283Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

14-24839270-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839270
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839270
    reference: chr 14
allele count: 2
allele frequency: 1.767159115006715e-5
allele num: 113176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+394T>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.705T>G
  hgvsp: ENST00000555590.1:c.705T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.705T>G
  hgvsp: ENST00000424781.2:c.705T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.456T>G
  hgvsp: ENST00000554344.1:c.456T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.456T>G
  hgvsp: ENST00000557451.1:c.456T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.456T>G
  hgvsp: ENST00000553879.1:c.456T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.855T>G
  hgvsp: ENST00000554591.1:c.855T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.630T>G
  hgvsp: ENST00000422617.3:c.630T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.630T>G
  hgvsp: ENST00000556169.1:c.630T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.630T>G
  hgvsp: ENST00000555453.1:c.630T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.762T>G
  hgvsp: ENST00000553469.1:c.762T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.705T>G
  hgvsp: ENST00000554966.1:c.705T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.666T>G
  hgvsp: ENST00000554050.1:c.666T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.762T>G
  hgvsp: ENST00000539237.2:c.762T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.866T>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.787T>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.665T>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.762T>G
  hgvsp: ENST00000556279.1:c.762T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.666T>G
  hgvsp: ENST00000250373.4:c.666T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro285Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

14-24839271-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839271
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839271
    reference: chr 14
allele count: 48
allele frequency: 4.243956782373433e-4
allele num: 113102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.706C>T
  hgvsp: ENSP00000451224.1:p.Arg236Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.666C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.788C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+395C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.667C>T
  hgvsp: ENSP00000450590.1:p.Arg223Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.856C>T
  hgvsp: ENSP00000452039.1:p.Arg286Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.706C>T
  hgvsp: ENSP00000450644.1:p.Arg236Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.763C>T
  hgvsp: ENSP00000452270.1:p.Arg255Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+395C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.763C>T
  hgvsp: ENSP00000439350.2:p.Arg255Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.631C>T
  hgvsp: ENSP00000451454.1:p.Arg211Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.457C>T
  hgvsp: ENSP00000450733.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.457C>T
  hgvsp: ENSP00000452349.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.856C>T
  hgvsp: ENSP00000388910.2:p.Arg286Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.457C>T
  hgvsp: ENSP00000451284.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.763C>T
  hgvsp: ENSP00000451502.1:p.Arg255Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.457C>T
  hgvsp: ENSP00000450469.1:p.Arg153Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.667C>T
  hgvsp: ENSP00000451151.1:p.Arg223Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.667C>T
  hgvsp: ENSP00000250373.4:p.Arg223Trp
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg286Trp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-24839281-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839281
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839281
    reference: chr 14
allele count: 155
allele frequency: 1.369669335312726e-3
allele num: 113166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.866C>A
  hgvsp: ENSP00000452039.1:p.Thr289Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.641C>A
  hgvsp: ENSP00000451454.1:p.Thr214Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.467C>A
  hgvsp: ENSP00000452349.1:p.Thr156Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.467C>A
  hgvsp: ENSP00000450469.1:p.Thr156Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.716C>A
  hgvsp: ENSP00000450644.1:p.Thr239Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.677C>A
  hgvsp: ENSP00000250373.4:p.Thr226Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.677C>A
  hgvsp: ENSP00000451151.1:p.Thr226Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.716C>A
  hgvsp: ENSP00000388668.2:p.Thr239Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.773C>A
  hgvsp: ENSP00000439350.2:p.Thr258Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.773C>A
  hgvsp: ENSP00000452270.1:p.Thr258Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.641C>A
  hgvsp: ENSP00000450686.1:p.Thr214Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.773C>A
  hgvsp: ENSP00000451502.1:p.Thr258Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.676C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.716C>A
  hgvsp: ENSP00000451224.1:p.Thr239Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.677C>A
  hgvsp: ENSP00000450590.1:p.Thr226Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.866C>A
  hgvsp: ENSP00000388910.2:p.Thr289Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.798C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+405C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.467C>A
  hgvsp: ENSP00000451284.1:p.Thr156Asn
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr289Asn
num of homozygotes: 1
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-24839286-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839286
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839286
    reference: chr 14
allele count: 8
allele frequency: 7.074762553281805e-5
allele num: 113078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.646G>A
  hgvsp: ENSP00000451454.1:p.Glu216Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.681G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.472G>A
  hgvsp: ENSP00000450469.1:p.Glu158Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.975G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.721G>A
  hgvsp: ENSP00000388668.2:p.Glu241Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.682G>A
  hgvsp: ENSP00000450590.1:p.Glu228Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.803G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.778G>A
  hgvsp: ENSP00000439350.2:p.Glu260Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.721G>A
  hgvsp: ENSP00000451224.1:p.Glu241Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.472G>A
  hgvsp: ENSP00000452349.1:p.Glu158Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.682G>A
  hgvsp: ENSP00000451151.1:p.Glu228Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.871G>A
  hgvsp: ENSP00000452039.1:p.Glu291Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.721G>A
  hgvsp: ENSP00000450644.1:p.Glu241Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.778G>A
  hgvsp: ENSP00000452270.1:p.Glu260Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.871G>A
  hgvsp: ENSP00000388910.2:p.Glu291Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.646G>A
  hgvsp: ENSP00000396788.3:p.Glu216Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.882G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.778G>A
  hgvsp: ENSP00000451502.1:p.Glu260Lys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+410G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.472G>A
  hgvsp: ENSP00000451284.1:p.Glu158Lys
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu291Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

14-24839292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839292
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839292
    reference: chr 14
allele count: 3
allele frequency: 2.651535238903325e-5
allele num: 113142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.478C>T
  hgvsp: ENSP00000450469.1:p.Pro160Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.652C>T
  hgvsp: ENSP00000396788.3:p.Pro218Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.727C>T
  hgvsp: ENSP00000450644.1:p.Pro243Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.888C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.688C>T
  hgvsp: ENSP00000451151.1:p.Pro230Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.877C>T
  hgvsp: ENSP00000452039.1:p.Pro293Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+416C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.727C>T
  hgvsp: ENSP00000388668.2:p.Pro243Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.784C>T
  hgvsp: ENSP00000452270.1:p.Pro262Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.652C>T
  hgvsp: ENSP00000451454.1:p.Pro218Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.784C>T
  hgvsp: ENSP00000439350.2:p.Pro262Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.784C>T
  hgvsp: ENSP00000451502.1:p.Pro262Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.478C>T
  hgvsp: ENSP00000450733.1:p.Pro160Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.478C>T
  hgvsp: ENSP00000452349.1:p.Pro160Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.652C>T
  hgvsp: ENSP00000450686.1:p.Pro218Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.688C>T
  hgvsp: ENSP00000450590.1:p.Pro230Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.727C>T
  hgvsp: ENSP00000451224.1:p.Pro243Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.981C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.688C>T
  hgvsp: ENSP00000250373.4:p.Pro230Ser
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro293Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-24839299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839299
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839299
    reference: chr 14
allele count: 1
allele frequency: 8.847208705653366e-6
allele num: 113030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.659G>A
  hgvsp: ENSP00000396788.3:p.Ser220Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.694G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.695G>A
  hgvsp: ENSP00000250373.4:p.Ser232Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.485G>A
  hgvsp: ENSP00000450469.1:p.Ser162Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.485G>A
  hgvsp: ENSP00000452349.1:p.Ser162Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+423G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.791G>A
  hgvsp: ENSP00000451502.1:p.Ser264Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.734G>A
  hgvsp: ENSP00000388668.2:p.Ser245Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.485G>A
  hgvsp: ENSP00000451284.1:p.Ser162Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.734G>A
  hgvsp: ENSP00000451224.1:p.Ser245Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.791G>A
  hgvsp: ENSP00000452270.1:p.Ser264Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.988G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.695G>A
  hgvsp: ENSP00000450590.1:p.Ser232Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.659G>A
  hgvsp: ENSP00000450686.1:p.Ser220Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.734G>A
  hgvsp: ENSP00000450644.1:p.Ser245Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.659G>A
  hgvsp: ENSP00000451454.1:p.Ser220Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.884G>A
  hgvsp: ENSP00000452039.1:p.Ser295Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.791G>A
  hgvsp: ENSP00000439350.2:p.Ser264Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.884G>A
  hgvsp: ENSP00000388910.2:p.Ser295Asn
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser295Asn
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

14-24839300-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839300
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839300
    reference: chr 14
allele count: 1
allele frequency: 8.847365254627173e-6
allele num: 113028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.695C>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.486C>G
  hgvsp: ENSP00000450469.1:p.Ser162Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.989C>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.817C>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.885C>G
  hgvsp: ENSP00000388910.2:p.Ser295Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.792C>G
  hgvsp: ENSP00000451502.1:p.Ser264Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.660C>G
  hgvsp: ENSP00000450686.1:p.Ser220Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.885C>G
  hgvsp: ENSP00000452039.1:p.Ser295Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.696C>G
  hgvsp: ENSP00000450590.1:p.Ser232Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.896C>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.696C>G
  hgvsp: ENSP00000451151.1:p.Ser232Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.486C>G
  hgvsp: ENSP00000452349.1:p.Ser162Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.792C>G
  hgvsp: ENSP00000452270.1:p.Ser264Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.735C>G
  hgvsp: ENSP00000451224.1:p.Ser245Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+424C>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.735C>G
  hgvsp: ENSP00000388668.2:p.Ser245Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.660C>G
  hgvsp: ENSP00000396788.3:p.Ser220Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+424C>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.792C>G
  hgvsp: ENSP00000439350.2:p.Ser264Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.486C>G
  hgvsp: ENSP00000451284.1:p.Ser162Arg
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser295Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

14-24839303-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839303
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839303
    reference: chr 14
allele count: 4
allele frequency: 3.540136295247367e-5
allele num: 112990
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.663G>C
  hgvsp: ENST00000556169.1:c.663G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.738G>C
  hgvsp: ENST00000424781.2:c.738G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.820G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.888G>C
  hgvsp: ENST00000413692.2:c.888G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+427G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+427G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.795G>C
  hgvsp: ENST00000556279.1:c.795G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.489G>C
  hgvsp: ENST00000554661.1:c.489G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.699G>C
  hgvsp: ENST00000554050.1:c.699G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.888G>C
  hgvsp: ENST00000554591.1:c.888G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.992G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.663G>C
  hgvsp: ENST00000422617.3:c.663G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.738G>C
  hgvsp: ENST00000554966.1:c.738G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.489G>C
  hgvsp: ENST00000557451.1:c.489G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.489G>C
  hgvsp: ENST00000553879.1:c.489G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.795G>C
  hgvsp: ENST00000553469.1:c.795G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.489G>C
  hgvsp: ENST00000554344.1:c.489G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.899G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.795G>C
  hgvsp: ENST00000539237.2:c.795G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.699G>C
  hgvsp: ENST00000250373.4:c.699G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu296Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

14-24839306-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839306
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839306
    reference: chr 14
allele count: 1
allele frequency: 8.850184083828943e-6
allele num: 112992
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.741T>C
  hgvsp: ENST00000424781.2:c.741T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.702T>C
  hgvsp: ENST00000250373.4:c.702T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.666T>C
  hgvsp: ENST00000555453.1:c.666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.702T>C
  hgvsp: ENST00000553708.1:c.702T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.492T>C
  hgvsp: ENST00000554661.1:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.823T>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.902T>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.492T>C
  hgvsp: ENST00000553879.1:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.798T>C
  hgvsp: ENST00000553469.1:c.798T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.891T>C
  hgvsp: ENST00000554591.1:c.891T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+430T>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.741T>C
  hgvsp: ENST00000555590.1:c.741T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.798T>C
  hgvsp: ENST00000556279.1:c.798T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.492T>C
  hgvsp: ENST00000557451.1:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.666T>C
  hgvsp: ENST00000422617.3:c.666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.798T>C
  hgvsp: ENST00000539237.2:c.798T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.891T>C
  hgvsp: ENST00000413692.2:c.891T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.492T>C
  hgvsp: ENST00000554344.1:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.995T>C
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Tyr297Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/14-24839315-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839315
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839315
    reference: chr 14
allele count: 1
allele frequency: 8.883677131638327e-6
allele num: 112566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.711C>A
  hgvsp: ENSP00000450590.1:p.Ser237Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.750C>A
  hgvsp: ENSP00000450644.1:p.Ser250Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.750C>A
  hgvsp: ENSP00000388668.2:p.Ser250Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1004C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+439C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.911C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.501C>A
  hgvsp: ENSP00000450733.1:p.Ser167Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.501C>A
  hgvsp: ENSP00000452349.1:p.Ser167Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.807C>A
  hgvsp: ENSP00000452270.1:p.Ser269Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.675C>A
  hgvsp: ENSP00000451454.1:p.Ser225Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.900C>A
  hgvsp: ENSP00000452039.1:p.Ser300Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.807C>A
  hgvsp: ENSP00000439350.2:p.Ser269Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.711C>A
  hgvsp: ENSP00000451151.1:p.Ser237Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.750C>A
  hgvsp: ENSP00000451224.1:p.Ser250Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.711C>A
  hgvsp: ENSP00000250373.4:p.Ser237Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.501C>A
  hgvsp: ENSP00000450469.1:p.Ser167Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.900C>A
  hgvsp: ENSP00000388910.2:p.Ser300Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.675C>A
  hgvsp: ENSP00000396788.3:p.Ser225Arg
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.501C>A
  hgvsp: ENSP00000451284.1:p.Ser167Arg
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser300Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

14-24839318-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839318
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839318
    reference: chr 14
allele count: 2
allele frequency: 1.77818873695254e-5
allele num: 112474
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.810C>T
  hgvsp: ENST00000553469.1:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.810C>T
  hgvsp: ENST00000556279.1:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.678C>T
  hgvsp: ENST00000556169.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.903C>T
  hgvsp: ENST00000554591.1:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.713C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.753C>T
  hgvsp: ENST00000554966.1:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.714C>T
  hgvsp: ENST00000553708.1:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.914C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.753C>T
  hgvsp: ENST00000424781.2:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.678C>T
  hgvsp: ENST00000422617.3:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.714C>T
  hgvsp: ENST00000554050.1:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+442C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.504C>T
  hgvsp: ENST00000554344.1:c.504C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.504C>T
  hgvsp: ENST00000557451.1:c.504C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.504C>T
  hgvsp: ENST00000553879.1:c.504C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.810C>T
  hgvsp: ENST00000539237.2:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1007C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.678C>T
  hgvsp: ENST00000555453.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.714C>T
  hgvsp: ENST00000250373.4:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro301Pro
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

14-24839326-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839326
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839326
    reference: chr 14
allele count: 2
allele frequency: 1.779264452075512e-5
allele num: 112406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.911G>A
  hgvsp: ENSP00000388910.2:p.Arg304Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.686G>A
  hgvsp: ENSP00000450686.1:p.Arg229Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.512G>A
  hgvsp: ENSP00000450733.1:p.Arg171Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.843G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.761G>A
  hgvsp: ENSP00000388668.2:p.Arg254Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.761G>A
  hgvsp: ENSP00000450644.1:p.Arg254Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.922G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.722G>A
  hgvsp: ENSP00000250373.4:p.Arg241Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.686G>A
  hgvsp: ENSP00000396788.3:p.Arg229Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+450G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.686G>A
  hgvsp: ENSP00000451454.1:p.Arg229Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.512G>A
  hgvsp: ENSP00000452349.1:p.Arg171Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.911G>A
  hgvsp: ENSP00000452039.1:p.Arg304Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.761G>A
  hgvsp: ENSP00000451224.1:p.Arg254Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+450G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.722G>A
  hgvsp: ENSP00000451151.1:p.Arg241Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.818G>A
  hgvsp: ENSP00000451502.1:p.Arg273Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.818G>A
  hgvsp: ENSP00000452270.1:p.Arg273Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.512G>A
  hgvsp: ENSP00000450469.1:p.Arg171Gln
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg304Gln
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

14-24839339-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839339
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839339
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 112588
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.525T>G
  hgvsp: ENSP00000452349.1:p.Asp175Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1028T>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.924T>G
  hgvsp: ENSP00000388910.2:p.Asp308Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.774T>G
  hgvsp: ENSP00000388668.2:p.Asp258Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.735T>G
  hgvsp: ENSP00000451151.1:p.Asp245Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.831T>G
  hgvsp: ENSP00000452270.1:p.Asp277Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+463T>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.924T>G
  hgvsp: ENSP00000452039.1:p.Asp308Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.699T>G
  hgvsp: ENSP00000396788.3:p.Asp233Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.525T>G
  hgvsp: ENSP00000451284.1:p.Asp175Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.774T>G
  hgvsp: ENSP00000450644.1:p.Asp258Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.735T>G
  hgvsp: ENSP00000450590.1:p.Asp245Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.525T>G
  hgvsp: ENSP00000450469.1:p.Asp175Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.735T>G
  hgvsp: ENSP00000250373.4:p.Asp245Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.831T>G
  hgvsp: ENSP00000439350.2:p.Asp277Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.699T>G
  hgvsp: ENSP00000451454.1:p.Asp233Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.525T>G
  hgvsp: ENSP00000450733.1:p.Asp175Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.774T>G
  hgvsp: ENSP00000451224.1:p.Asp258Glu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+463T>G
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp308Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

14-24839341-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839341
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839341
    reference: chr 14
allele count: 123
allele frequency: 1.093488851747804e-3
allele num: 112484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.737G>A
  hgvsp: ENSP00000450590.1:p.Ser246Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.858G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.926G>A
  hgvsp: ENSP00000388910.2:p.Ser309Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.527G>A
  hgvsp: ENSP00000451284.1:p.Ser176Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.701G>A
  hgvsp: ENSP00000396788.3:p.Ser234Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.701G>A
  hgvsp: ENSP00000450686.1:p.Ser234Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+465G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.527G>A
  hgvsp: ENSP00000450733.1:p.Ser176Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.776G>A
  hgvsp: ENSP00000450644.1:p.Ser259Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.776G>A
  hgvsp: ENSP00000388668.2:p.Ser259Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1030G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.737G>A
  hgvsp: ENSP00000451151.1:p.Ser246Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.926G>A
  hgvsp: ENSP00000452039.1:p.Ser309Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.527G>A
  hgvsp: ENSP00000452349.1:p.Ser176Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.776G>A
  hgvsp: ENSP00000451224.1:p.Ser259Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.527G>A
  hgvsp: ENSP00000450469.1:p.Ser176Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.833G>A
  hgvsp: ENSP00000451502.1:p.Ser278Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.833G>A
  hgvsp: ENSP00000452270.1:p.Ser278Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.701G>A
  hgvsp: ENSP00000451454.1:p.Ser234Asn
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser309Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

14-24839346-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839346
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839346
    reference: chr 14
allele count: 2
allele frequency: 1.779264452075512e-5
allele num: 112406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.532C>T
  hgvsp: ENST00000554661.1:c.532C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.706C>T
  hgvsp: ENST00000556169.1:c.706C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.863C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.942C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.781C>T
  hgvsp: ENST00000554966.1:c.781C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.706C>T
  hgvsp: ENST00000422617.3:c.706C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.742C>T
  hgvsp: ENST00000553708.1:c.742C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.781C>T
  hgvsp: ENST00000555590.1:c.781C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.838C>T
  hgvsp: ENST00000556279.1:c.838C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.532C>T
  hgvsp: ENST00000557451.1:c.532C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.931C>T
  hgvsp: ENST00000554591.1:c.931C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.741C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+470C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.742C>T
  hgvsp: ENST00000554050.1:c.742C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.742C>T
  hgvsp: ENST00000250373.4:c.742C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.532C>T
  hgvsp: ENST00000554344.1:c.532C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.706C>T
  hgvsp: ENST00000555453.1:c.706C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.838C>T
  hgvsp: ENST00000539237.2:c.838C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1035C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+470C>T
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu311Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

14-24839354-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839354
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839354
    reference: chr 14
allele count: 1
allele frequency: 8.919651776794634e-6
allele num: 112112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.789C>T
  hgvsp: ENST00000555590.1:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.540C>T
  hgvsp: ENST00000553879.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.846C>T
  hgvsp: ENST00000556279.1:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.750C>T
  hgvsp: ENST00000554050.1:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.789C>T
  hgvsp: ENST00000424781.2:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.750C>T
  hgvsp: ENST00000250373.4:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.789C>T
  hgvsp: ENST00000554966.1:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.871C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.939C>T
  hgvsp: ENST00000554591.1:c.939C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.950C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.540C>T
  hgvsp: ENST00000554344.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.540C>T
  hgvsp: ENST00000557451.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.750C>T
  hgvsp: ENST00000553708.1:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.749C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.540C>T
  hgvsp: ENST00000554661.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.846C>T
  hgvsp: ENST00000539237.2:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.714C>T
  hgvsp: ENST00000555453.1:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1043C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.714C>T
  hgvsp: ENST00000422617.3:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu313Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

14-24839368-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839368
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839368
    reference: chr 14
allele count: 1
allele frequency: 8.898063781321184e-6
allele num: 112384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.728C>T
  hgvsp: ENSP00000396788.3:p.Pro243Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.803C>T
  hgvsp: ENSP00000450644.1:p.Pro268Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.964C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.803C>T
  hgvsp: ENSP00000451224.1:p.Pro268Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.764C>T
  hgvsp: ENSP00000451151.1:p.Pro255Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.803C>T
  hgvsp: ENSP00000388668.2:p.Pro268Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.860C>T
  hgvsp: ENSP00000452270.1:p.Pro287Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.728C>T
  hgvsp: ENSP00000450686.1:p.Pro243Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.728C>T
  hgvsp: ENSP00000451454.1:p.Pro243Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+492C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.764C>T
  hgvsp: ENSP00000450590.1:p.Pro255Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.953C>T
  hgvsp: ENSP00000452039.1:p.Pro318Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.554C>T
  hgvsp: ENSP00000452349.1:p.Pro185Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.554C>T
  hgvsp: ENSP00000450469.1:p.Pro185Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.763C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.885C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.554C>T
  hgvsp: ENSP00000450733.1:p.Pro185Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1057C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+492C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.764C>T
  hgvsp: ENSP00000250373.4:p.Pro255Leu
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro318Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

14-24839373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839373
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839373
    reference: chr 14
allele count: 3
allele frequency: 2.665529374133703e-5
allele num: 112548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.958C>T
  hgvsp: ENSP00000452039.1:p.Pro320Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.808C>T
  hgvsp: ENSP00000451224.1:p.Pro270Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.733C>T
  hgvsp: ENSP00000451454.1:p.Pro245Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.808C>T
  hgvsp: ENSP00000388668.2:p.Pro270Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.733C>T
  hgvsp: ENSP00000396788.3:p.Pro245Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.969C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.733C>T
  hgvsp: ENSP00000450686.1:p.Pro245Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.769C>T
  hgvsp: ENSP00000250373.4:p.Pro257Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.865C>T
  hgvsp: ENSP00000451502.1:p.Pro289Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.559C>T
  hgvsp: ENSP00000451284.1:p.Pro187Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.865C>T
  hgvsp: ENSP00000452270.1:p.Pro289Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.559C>T
  hgvsp: ENSP00000452349.1:p.Pro187Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+497C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.769C>T
  hgvsp: ENSP00000450590.1:p.Pro257Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.808C>T
  hgvsp: ENSP00000450644.1:p.Pro270Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.559C>T
  hgvsp: ENSP00000450469.1:p.Pro187Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.559C>T
  hgvsp: ENSP00000450733.1:p.Pro187Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.958C>T
  hgvsp: ENSP00000388910.2:p.Pro320Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.890C>T
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro320Ser
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

14-24839377-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839377
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839377
    reference: chr 14
allele count: 1
allele frequency: 8.877368037924116e-6
allele num: 112646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.812C>T
  hgvsp: ENSP00000451224.1:p.Ala271Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.869C>T
  hgvsp: ENSP00000452270.1:p.Ala290Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.563C>T
  hgvsp: ENSP00000452349.1:p.Ala188Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.737C>T
  hgvsp: ENSP00000396788.3:p.Ala246Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.869C>T
  hgvsp: ENSP00000451502.1:p.Ala290Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.772C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.773C>T
  hgvsp: ENSP00000250373.4:p.Ala258Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.737C>T
  hgvsp: ENSP00000450686.1:p.Ala246Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.563C>T
  hgvsp: ENSP00000451284.1:p.Ala188Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.894C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.812C>T
  hgvsp: ENSP00000388668.2:p.Ala271Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.812C>T
  hgvsp: ENSP00000450644.1:p.Ala271Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.563C>T
  hgvsp: ENSP00000450469.1:p.Ala188Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.737C>T
  hgvsp: ENSP00000451454.1:p.Ala246Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.869C>T
  hgvsp: ENSP00000439350.2:p.Ala290Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.962C>T
  hgvsp: ENSP00000452039.1:p.Ala321Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.563C>T
  hgvsp: ENSP00000450733.1:p.Ala188Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.773C>T
  hgvsp: ENSP00000450590.1:p.Ala258Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.973C>T
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala321Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-24839383-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839383
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839383
    reference: chr 14
allele count: 1
allele frequency: 8.87342940299567e-6
allele num: 112696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.875C>A
  hgvsp: ENSP00000439350.2:p.Pro292Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1072C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.569C>A
  hgvsp: ENSP00000450469.1:p.Pro190Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.818C>A
  hgvsp: ENSP00000450644.1:p.Pro273Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+507C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.818C>A
  hgvsp: ENSP00000451224.1:p.Pro273Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.779C>A
  hgvsp: ENSP00000450590.1:p.Pro260Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+507C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.968C>A
  hgvsp: ENSP00000452039.1:p.Pro323Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.569C>A
  hgvsp: ENSP00000451284.1:p.Pro190Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.875C>A
  hgvsp: ENSP00000452270.1:p.Pro292Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.779C>A
  hgvsp: ENSP00000451151.1:p.Pro260Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.569C>A
  hgvsp: ENSP00000450733.1:p.Pro190Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.778C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.875C>A
  hgvsp: ENSP00000451502.1:p.Pro292Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.818C>A
  hgvsp: ENSP00000388668.2:p.Pro273Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.569C>A
  hgvsp: ENSP00000452349.1:p.Pro190Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.743C>A
  hgvsp: ENSP00000450686.1:p.Pro248Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.979C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.968C>A
  hgvsp: ENSP00000388910.2:p.Pro323Gln
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro323Gln
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-24839384-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839384
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839384
    reference: chr 14
allele count: 1
allele frequency: 8.862576882854458e-6
allele num: 112834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.570G>A
  hgvsp: ENST00000553879.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.570G>A
  hgvsp: ENST00000554344.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.876G>A
  hgvsp: ENST00000553469.1:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.744G>A
  hgvsp: ENST00000556169.1:c.744G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.876G>A
  hgvsp: ENST00000556279.1:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1073G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.570G>A
  hgvsp: ENST00000557451.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.876G>A
  hgvsp: ENST00000539237.2:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.819G>A
  hgvsp: ENST00000555590.1:c.819G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.980G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.780G>A
  hgvsp: ENST00000250373.4:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+508G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.969G>A
  hgvsp: ENST00000413692.2:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.780G>A
  hgvsp: ENST00000554050.1:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.780G>A
  hgvsp: ENST00000553708.1:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.819G>A
  hgvsp: ENST00000424781.2:c.819G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.901G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.969G>A
  hgvsp: ENST00000554591.1:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.744G>A
  hgvsp: ENST00000422617.3:c.744G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro323Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/14-24839385-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839385
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839385
    reference: chr 14
allele count: 6
allele frequency: 5.316226896563945e-5
allele num: 112862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.820C>A
  hgvsp: ENST00000554966.1:c.820C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.970C>A
  hgvsp: ENST00000554591.1:c.970C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.781C>A
  hgvsp: ENST00000554050.1:c.781C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.745C>A
  hgvsp: ENST00000555453.1:c.745C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.745C>A
  hgvsp: ENST00000556169.1:c.745C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.781C>A
  hgvsp: ENST00000553708.1:c.781C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.877C>A
  hgvsp: ENST00000556279.1:c.877C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.981C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.970C>A
  hgvsp: ENST00000413692.2:c.970C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.780C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.571C>A
  hgvsp: ENST00000557451.1:c.571C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.820C>A
  hgvsp: ENST00000555590.1:c.820C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.902C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.745C>A
  hgvsp: ENST00000422617.3:c.745C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.781C>A
  hgvsp: ENST00000250373.4:c.781C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.877C>A
  hgvsp: ENST00000553469.1:c.877C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.571C>A
  hgvsp: ENST00000553879.1:c.571C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.820C>A
  hgvsp: ENST00000424781.2:c.820C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.571C>A
  hgvsp: ENST00000554344.1:c.571C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg324Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

14-24839385-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839385
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839385
    reference: chr 14
allele count: 1
allele frequency: 8.86037816093991e-6
allele num: 112862
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.820C>T
  hgvsp: ENSP00000388668.2:p.Arg274Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.970C>T
  hgvsp: ENSP00000452039.1:p.Arg324Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.781C>T
  hgvsp: ENSP00000451151.1:p.Arg261Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.877C>T
  hgvsp: ENSP00000451502.1:p.Arg293Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.571C>T
  hgvsp: ENSP00000452349.1:p.Arg191Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.745C>T
  hgvsp: ENSP00000450686.1:p.Arg249Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.571C>T
  hgvsp: ENSP00000450733.1:p.Arg191Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.781C>T
  hgvsp: ENSP00000450590.1:p.Arg261Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.820C>T
  hgvsp: ENSP00000451224.1:p.Arg274Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.820C>T
  hgvsp: ENSP00000450644.1:p.Arg274Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.877C>T
  hgvsp: ENSP00000452270.1:p.Arg293Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.970C>T
  hgvsp: ENSP00000388910.2:p.Arg324Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.780C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.571C>T
  hgvsp: ENSP00000450469.1:p.Arg191Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.781C>T
  hgvsp: ENSP00000250373.4:p.Arg261Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.571C>T
  hgvsp: ENSP00000451284.1:p.Arg191Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.877C>T
  hgvsp: ENSP00000439350.2:p.Arg293Trp
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.981C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+509C>T
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg324Trp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

14-24839386-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839386
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839386
    reference: chr 14
allele count: 2
allele frequency: 1.768221522792375e-5
allele num: 113108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.971G>A
  hgvsp: ENSP00000452039.1:p.Arg324Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1075G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.821G>A
  hgvsp: ENSP00000451224.1:p.Arg274Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.572G>A
  hgvsp: ENSP00000451284.1:p.Arg191Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.746G>A
  hgvsp: ENSP00000450686.1:p.Arg249Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.878G>A
  hgvsp: ENSP00000439350.2:p.Arg293Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.572G>A
  hgvsp: ENSP00000452349.1:p.Arg191Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.746G>A
  hgvsp: ENSP00000396788.3:p.Arg249Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.903G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.782G>A
  hgvsp: ENSP00000451151.1:p.Arg261Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.746G>A
  hgvsp: ENSP00000451454.1:p.Arg249Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.971G>A
  hgvsp: ENSP00000388910.2:p.Arg324Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.572G>A
  hgvsp: ENSP00000450733.1:p.Arg191Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.878G>A
  hgvsp: ENSP00000452270.1:p.Arg293Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.572G>A
  hgvsp: ENSP00000450469.1:p.Arg191Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.821G>A
  hgvsp: ENSP00000450644.1:p.Arg274Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+510G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.821G>A
  hgvsp: ENSP00000388668.2:p.Arg274Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+510G>A
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg324Gln
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

14-24839387-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839387
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839387
    reference: chr 14
allele count: 8
allele frequency: 7.081902198930633e-5
allele num: 112964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.822G>A
  hgvsp: ENST00000555590.1:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.573G>A
  hgvsp: ENST00000554344.1:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.783G>A
  hgvsp: ENST00000553708.1:c.783G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.972G>A
  hgvsp: ENST00000554591.1:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.573G>A
  hgvsp: ENST00000553879.1:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.972G>A
  hgvsp: ENST00000413692.2:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.904G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.822G>A
  hgvsp: ENST00000424781.2:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.782G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.822G>A
  hgvsp: ENST00000554966.1:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.573G>A
  hgvsp: ENST00000554661.1:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.879G>A
  hgvsp: ENST00000539237.2:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1076G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.879G>A
  hgvsp: ENST00000553469.1:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.747G>A
  hgvsp: ENST00000555453.1:c.747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.747G>A
  hgvsp: ENST00000556169.1:c.747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.747G>A
  hgvsp: ENST00000422617.3:c.747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.879G>A
  hgvsp: ENST00000556279.1:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+511G>A
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg324Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

14-24839387-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839387
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839387
    reference: chr 14
allele count: 1
allele frequency: 8.852377748663291e-6
allele num: 112964
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.983G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.783G>C
  hgvsp: ENST00000554050.1:c.783G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.783G>C
  hgvsp: ENST00000553708.1:c.783G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.783G>C
  hgvsp: ENST00000250373.4:c.783G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.747G>C
  hgvsp: ENST00000555453.1:c.747G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.822G>C
  hgvsp: ENST00000424781.2:c.822G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.747G>C
  hgvsp: ENST00000422617.3:c.747G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.573G>C
  hgvsp: ENST00000553879.1:c.573G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.747G>C
  hgvsp: ENST00000556169.1:c.747G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.879G>C
  hgvsp: ENST00000539237.2:c.879G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.573G>C
  hgvsp: ENST00000554344.1:c.573G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.972G>C
  hgvsp: ENST00000554591.1:c.972G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.972G>C
  hgvsp: ENST00000413692.2:c.972G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.782G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.879G>C
  hgvsp: ENST00000553469.1:c.879G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.573G>C
  hgvsp: ENST00000554661.1:c.573G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+511G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1076G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+511G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.573G>C
  hgvsp: ENST00000557451.1:c.573G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg324Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

14-24839397-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839397
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839397
    reference: chr 14
allele count: 1
allele frequency: 8.775008775008775e-6
allele num: 113960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.793C>T
  hgvsp: ENSP00000451151.1:p.Pro265Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.583C>T
  hgvsp: ENSP00000450469.1:p.Pro195Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.583C>T
  hgvsp: ENSP00000452349.1:p.Pro195Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.914C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.982C>T
  hgvsp: ENSP00000388910.2:p.Pro328Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.832C>T
  hgvsp: ENSP00000388668.2:p.Pro278Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+521C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.792C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.832C>T
  hgvsp: ENSP00000451224.1:p.Pro278Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.982C>T
  hgvsp: ENSP00000452039.1:p.Pro328Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.889C>T
  hgvsp: ENSP00000451502.1:p.Pro297Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.583C>T
  hgvsp: ENSP00000450733.1:p.Pro195Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1086C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.889C>T
  hgvsp: ENSP00000452270.1:p.Pro297Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.583C>T
  hgvsp: ENSP00000451284.1:p.Pro195Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+521C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.832C>T
  hgvsp: ENSP00000450644.1:p.Pro278Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.889C>T
  hgvsp: ENSP00000439350.2:p.Pro297Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.757C>T
  hgvsp: ENSP00000451454.1:p.Pro253Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.793C>T
  hgvsp: ENSP00000250373.4:p.Pro265Ser
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro328Ser
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP

14-24839399-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839399
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839399
    reference: chr 14
allele count: 1
allele frequency: 8.765624726074227e-6
allele num: 114082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.585A>G
  hgvsp: ENST00000554661.1:c.585A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.834A>G
  hgvsp: ENST00000555590.1:c.834A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.795A>G
  hgvsp: ENST00000554050.1:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.834A>G
  hgvsp: ENST00000424781.2:c.834A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.585A>G
  hgvsp: ENST00000554344.1:c.585A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.834A>G
  hgvsp: ENST00000554966.1:c.834A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.891A>G
  hgvsp: ENST00000553469.1:c.891A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.891A>G
  hgvsp: ENST00000556279.1:c.891A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.759A>G
  hgvsp: ENST00000422617.3:c.759A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.984A>G
  hgvsp: ENST00000554591.1:c.984A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.759A>G
  hgvsp: ENST00000556169.1:c.759A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.585A>G
  hgvsp: ENST00000553879.1:c.585A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.984A>G
  hgvsp: ENST00000413692.2:c.984A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.795A>G
  hgvsp: ENST00000553708.1:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.795A>G
  hgvsp: ENST00000250373.4:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.891A>G
  hgvsp: ENST00000539237.2:c.891A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.916A>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.794A>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.585A>G
  hgvsp: ENST00000557451.1:c.585A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro328Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

14-24839414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839414
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839414
    reference: chr 14
allele count: 1
allele frequency: 8.711104916547614e-6
allele num: 114796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.600C>T
  hgvsp: ENST00000554344.1:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1103C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.849C>T
  hgvsp: ENST00000555590.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.906C>T
  hgvsp: ENST00000539237.2:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+538C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.906C>T
  hgvsp: ENST00000553469.1:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.810C>T
  hgvsp: ENST00000250373.4:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.774C>T
  hgvsp: ENST00000422617.3:c.774C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.906C>T
  hgvsp: ENST00000556279.1:c.906C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.999C>T
  hgvsp: ENST00000554591.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.849C>T
  hgvsp: ENST00000424781.2:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.810C>T
  hgvsp: ENST00000554050.1:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.810C>T
  hgvsp: ENST00000553708.1:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.849C>T
  hgvsp: ENST00000554966.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.774C>T
  hgvsp: ENST00000555453.1:c.774C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.809C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.600C>T
  hgvsp: ENST00000554661.1:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.600C>T
  hgvsp: ENST00000553879.1:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1010C>T
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg333Arg
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

14-24839422-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839422
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839422
    reference: chr 14
allele count: 1
allele frequency: 8.691722003963425e-6
allele num: 115052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.914G>A
  hgvsp: ENSP00000452270.1:p.Ser305Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.857G>A
  hgvsp: ENSP00000388668.2:p.Ser286Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.608G>A
  hgvsp: ENSP00000450469.1:p.Ser203Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.914G>A
  hgvsp: ENSP00000451502.1:p.Ser305Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.857G>A
  hgvsp: ENSP00000450644.1:p.Ser286Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.782G>A
  hgvsp: ENSP00000451454.1:p.Ser261Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.782G>A
  hgvsp: ENSP00000396788.3:p.Ser261Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.818G>A
  hgvsp: ENSP00000250373.4:p.Ser273Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.818G>A
  hgvsp: ENSP00000451151.1:p.Ser273Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.817G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+546G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.939G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.818G>A
  hgvsp: ENSP00000450590.1:p.Ser273Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.608G>A
  hgvsp: ENSP00000452349.1:p.Ser203Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.914G>A
  hgvsp: ENSP00000439350.2:p.Ser305Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1007G>A
  hgvsp: ENSP00000388910.2:p.Ser336Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1007G>A
  hgvsp: ENSP00000452039.1:p.Ser336Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.782G>A
  hgvsp: ENSP00000450686.1:p.Ser261Asn
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1018G>A
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser336Asn
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ

14-24839426-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839426
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839426
    reference: chr 14
allele count: 2
allele frequency: 1.7373477649021e-5
allele num: 115118
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.861G>C
  hgvsp: ENST00000424781.2:c.861G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.612G>C
  hgvsp: ENST00000557451.1:c.612G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.918G>C
  hgvsp: ENST00000556279.1:c.918G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.822G>C
  hgvsp: ENST00000250373.4:c.822G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.821G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.918G>C
  hgvsp: ENST00000553469.1:c.918G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1011G>C
  hgvsp: ENST00000554591.1:c.1011G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.861G>C
  hgvsp: ENST00000554966.1:c.861G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1115G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.612G>C
  hgvsp: ENST00000553879.1:c.612G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1011G>C
  hgvsp: ENST00000413692.2:c.1011G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.786G>C
  hgvsp: ENST00000555453.1:c.786G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.786G>C
  hgvsp: ENST00000422617.3:c.786G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+550G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.612G>C
  hgvsp: ENST00000554344.1:c.612G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.918G>C
  hgvsp: ENST00000539237.2:c.918G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.822G>C
  hgvsp: ENST00000554050.1:c.822G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.943G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.786G>C
  hgvsp: ENST00000556169.1:c.786G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser337Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

14-24839432-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839432
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839432
    reference: chr 14
allele count: 5
allele frequency: 4.332154987176821e-5
allele num: 115416
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.792C>G
  hgvsp: ENST00000422617.3:c.792C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1028C>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.618C>G
  hgvsp: ENST00000553879.1:c.618C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1017C>G
  hgvsp: ENST00000554591.1:c.1017C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.618C>G
  hgvsp: ENST00000554344.1:c.618C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.828C>G
  hgvsp: ENST00000250373.4:c.828C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.924C>G
  hgvsp: ENST00000556279.1:c.924C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.867C>G
  hgvsp: ENST00000424781.2:c.867C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.618C>G
  hgvsp: ENST00000554661.1:c.618C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.867C>G
  hgvsp: ENST00000554966.1:c.867C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.827C>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1017C>G
  hgvsp: ENST00000413692.2:c.1017C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.618C>G
  hgvsp: ENST00000557451.1:c.618C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.792C>G
  hgvsp: ENST00000555453.1:c.792C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.924C>G
  hgvsp: ENST00000539237.2:c.924C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+556C>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.867C>G
  hgvsp: ENST00000555590.1:c.867C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.828C>G
  hgvsp: ENST00000554050.1:c.828C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.792C>G
  hgvsp: ENST00000556169.1:c.792C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr339Thr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

14-24839442-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839442
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839442
    reference: chr 14
allele count: 1
allele frequency: 8.662808829134758e-6
allele num: 115436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.802G>A
  hgvsp: ENSP00000396788.3:p.Ala268Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1038G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.838G>A
  hgvsp: ENSP00000451151.1:p.Ala280Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1131G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.628G>A
  hgvsp: ENSP00000450733.1:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.628G>A
  hgvsp: ENSP00000450469.1:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1027G>A
  hgvsp: ENSP00000388910.2:p.Ala343Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.837G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.934G>A
  hgvsp: ENSP00000452270.1:p.Ala312Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.628G>A
  hgvsp: ENSP00000452349.1:p.Ala210Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1027G>A
  hgvsp: ENSP00000452039.1:p.Ala343Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.802G>A
  hgvsp: ENSP00000450686.1:p.Ala268Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.877G>A
  hgvsp: ENSP00000450644.1:p.Ala293Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.802G>A
  hgvsp: ENSP00000451454.1:p.Ala268Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.877G>A
  hgvsp: ENSP00000451224.1:p.Ala293Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.959G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.838G>A
  hgvsp: ENSP00000250373.4:p.Ala280Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.934G>A
  hgvsp: ENSP00000439350.2:p.Ala312Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.934G>A
  hgvsp: ENSP00000451502.1:p.Ala312Thr
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala343Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-24839442-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839442
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839442
    reference: chr 14
allele count: 1
allele frequency: 8.662808829134758e-6
allele num: 115436
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.838G>C
  hgvsp: ENSP00000250373.4:p.Ala280Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1131G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+566G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.628G>C
  hgvsp: ENSP00000450469.1:p.Ala210Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.877G>C
  hgvsp: ENSP00000451224.1:p.Ala293Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.628G>C
  hgvsp: ENSP00000452349.1:p.Ala210Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.959G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1027G>C
  hgvsp: ENSP00000452039.1:p.Ala343Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.838G>C
  hgvsp: ENSP00000450590.1:p.Ala280Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.802G>C
  hgvsp: ENSP00000396788.3:p.Ala268Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1027G>C
  hgvsp: ENSP00000388910.2:p.Ala343Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.934G>C
  hgvsp: ENSP00000452270.1:p.Ala312Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.877G>C
  hgvsp: ENSP00000388668.2:p.Ala293Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.628G>C
  hgvsp: ENSP00000450733.1:p.Ala210Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.838G>C
  hgvsp: ENSP00000451151.1:p.Ala280Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+566G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.934G>C
  hgvsp: ENSP00000439350.2:p.Ala312Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.802G>C
  hgvsp: ENSP00000450686.1:p.Ala268Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1038G>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.802G>C
  hgvsp: ENSP00000451454.1:p.Ala268Pro
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala343Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

14-24839443-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839443
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839443
    reference: chr 14
allele count: 4
allele frequency: 3.463443355383923e-5
allele num: 115492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.839C>T
  hgvsp: ENSP00000451151.1:p.Ala280Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.629C>T
  hgvsp: ENSP00000451284.1:p.Ala210Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.803C>T
  hgvsp: ENSP00000396788.3:p.Ala268Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1039C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.878C>T
  hgvsp: ENSP00000388668.2:p.Ala293Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.878C>T
  hgvsp: ENSP00000450644.1:p.Ala293Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.629C>T
  hgvsp: ENSP00000452349.1:p.Ala210Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.935C>T
  hgvsp: ENSP00000452270.1:p.Ala312Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1028C>T
  hgvsp: ENSP00000388910.2:p.Ala343Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.935C>T
  hgvsp: ENSP00000439350.2:p.Ala312Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.803C>T
  hgvsp: ENSP00000450686.1:p.Ala268Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+567C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.838C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.839C>T
  hgvsp: ENSP00000450590.1:p.Ala280Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.629C>T
  hgvsp: ENSP00000450469.1:p.Ala210Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+567C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.803C>T
  hgvsp: ENSP00000451454.1:p.Ala268Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.960C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.629C>T
  hgvsp: ENSP00000450733.1:p.Ala210Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.878C>T
  hgvsp: ENSP00000451224.1:p.Ala293Val
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala343Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

14-24839446-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839446
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839446
    reference: chr 14
allele count: 1
allele frequency: 8.654112434228745e-6
allele num: 115552
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.806C>T
  hgvsp: ENSP00000396788.3:p.Ser269Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1042C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.963C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+570C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1031C>T
  hgvsp: ENSP00000452039.1:p.Ser344Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.632C>T
  hgvsp: ENSP00000450733.1:p.Ser211Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1135C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.842C>T
  hgvsp: ENSP00000250373.4:p.Ser281Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.881C>T
  hgvsp: ENSP00000450644.1:p.Ser294Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.938C>T
  hgvsp: ENSP00000451502.1:p.Ser313Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.881C>T
  hgvsp: ENSP00000388668.2:p.Ser294Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.632C>T
  hgvsp: ENSP00000450469.1:p.Ser211Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.881C>T
  hgvsp: ENSP00000451224.1:p.Ser294Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.842C>T
  hgvsp: ENSP00000451151.1:p.Ser281Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.632C>T
  hgvsp: ENSP00000452349.1:p.Ser211Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.806C>T
  hgvsp: ENSP00000451454.1:p.Ser269Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.938C>T
  hgvsp: ENSP00000452270.1:p.Ser313Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.842C>T
  hgvsp: ENSP00000450590.1:p.Ser281Phe
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.841C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1031C>T
  hgvsp: ENSP00000388910.2:p.Ser344Phe
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser344Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

14-24839448-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839448
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839448
    reference: chr 14
allele count: 1
allele frequency: 8.662058451570432e-6
allele num: 115446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.965C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.634C>T
  hgvsp: ENSP00000452349.1:p.Pro212Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.634C>T
  hgvsp: ENSP00000450469.1:p.Pro212Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+572C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.940C>T
  hgvsp: ENSP00000439350.2:p.Pro314Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.808C>T
  hgvsp: ENSP00000396788.3:p.Pro270Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+572C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.844C>T
  hgvsp: ENSP00000451151.1:p.Pro282Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.843C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.883C>T
  hgvsp: ENSP00000450644.1:p.Pro295Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.808C>T
  hgvsp: ENSP00000451454.1:p.Pro270Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.883C>T
  hgvsp: ENSP00000388668.2:p.Pro295Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.844C>T
  hgvsp: ENSP00000250373.4:p.Pro282Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1033C>T
  hgvsp: ENSP00000452039.1:p.Pro345Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.940C>T
  hgvsp: ENSP00000452270.1:p.Pro314Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.634C>T
  hgvsp: ENSP00000450733.1:p.Pro212Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1033C>T
  hgvsp: ENSP00000388910.2:p.Pro345Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.808C>T
  hgvsp: ENSP00000450686.1:p.Pro270Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.883C>T
  hgvsp: ENSP00000451224.1:p.Pro295Ser
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro345Ser
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

14-24839457-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839457
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839457
    reference: chr 14
allele count: 1
allele frequency: 8.672124323574303e-6
allele num: 115312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.817T>C
  hgvsp: ENSP00000450686.1:p.Ser273Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.949T>C
  hgvsp: ENSP00000452270.1:p.Ser317Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.892T>C
  hgvsp: ENSP00000388668.2:p.Ser298Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.853T>C
  hgvsp: ENSP00000451151.1:p.Ser285Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1042T>C
  hgvsp: ENSP00000388910.2:p.Ser348Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+581T>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.817T>C
  hgvsp: ENSP00000451454.1:p.Ser273Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.643T>C
  hgvsp: ENSP00000452349.1:p.Ser215Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.853T>C
  hgvsp: ENSP00000450590.1:p.Ser285Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.892T>C
  hgvsp: ENSP00000450644.1:p.Ser298Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1053T>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.949T>C
  hgvsp: ENSP00000451502.1:p.Ser317Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1042T>C
  hgvsp: ENSP00000452039.1:p.Ser348Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.853T>C
  hgvsp: ENSP00000250373.4:p.Ser285Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.643T>C
  hgvsp: ENSP00000450469.1:p.Ser215Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.817T>C
  hgvsp: ENSP00000396788.3:p.Ser273Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.892T>C
  hgvsp: ENSP00000451224.1:p.Ser298Pro
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.852T>C
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.949T>C
  hgvsp: ENSP00000439350.2:p.Ser317Pro
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser348Pro
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/14-24839463-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839463
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839463
    reference: chr 14
allele count: 1
allele frequency: 8.657259111765215e-6
allele num: 115510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.898C>A
  hgvsp: ENSP00000451224.1:p.Arg300Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.823C>A
  hgvsp: ENSP00000396788.3:p.Arg275Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.898C>A
  hgvsp: ENSP00000388668.2:p.Arg300Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1152C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.955C>A
  hgvsp: ENSP00000452270.1:p.Arg319Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.955C>A
  hgvsp: ENSP00000451502.1:p.Arg319Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.859C>A
  hgvsp: ENSP00000250373.4:p.Arg287Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.823C>A
  hgvsp: ENSP00000451454.1:p.Arg275Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.649C>A
  hgvsp: ENSP00000452349.1:p.Arg217Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.649C>A
  hgvsp: ENSP00000450469.1:p.Arg217Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+587C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.649C>A
  hgvsp: ENSP00000450733.1:p.Arg217Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.980C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.859C>A
  hgvsp: ENSP00000451151.1:p.Arg287Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.823C>A
  hgvsp: ENSP00000450686.1:p.Arg275Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.898C>A
  hgvsp: ENSP00000450644.1:p.Arg300Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.859C>A
  hgvsp: ENSP00000450590.1:p.Arg287Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+587C>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1048C>A
  hgvsp: ENSP00000452039.1:p.Arg350Ser
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg350Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

14-24839463-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839463
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839463
    reference: chr 14
allele count: 2
allele frequency: 1.731451822353043e-5
allele num: 115510
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.980C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.823C>T
  hgvsp: ENSP00000450686.1:p.Arg275Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1059C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.823C>T
  hgvsp: ENSP00000451454.1:p.Arg275Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.955C>T
  hgvsp: ENSP00000439350.2:p.Arg319Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.955C>T
  hgvsp: ENSP00000452270.1:p.Arg319Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.649C>T
  hgvsp: ENSP00000452349.1:p.Arg217Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.898C>T
  hgvsp: ENSP00000388668.2:p.Arg300Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.649C>T
  hgvsp: ENSP00000450469.1:p.Arg217Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.859C>T
  hgvsp: ENSP00000450590.1:p.Arg287Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1152C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.823C>T
  hgvsp: ENSP00000396788.3:p.Arg275Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.858C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1048C>T
  hgvsp: ENSP00000452039.1:p.Arg350Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1048C>T
  hgvsp: ENSP00000388910.2:p.Arg350Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.859C>T
  hgvsp: ENSP00000451151.1:p.Arg287Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.649C>T
  hgvsp: ENSP00000450733.1:p.Arg217Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+587C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.859C>T
  hgvsp: ENSP00000250373.4:p.Arg287Cys
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.898C>T
  hgvsp: ENSP00000450644.1:p.Arg300Cys
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg350Cys
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

14-24839474-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839474
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839474
    reference: chr 14
allele count: 1
allele frequency: 8.643789437289307e-6
allele num: 115690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.909G>T
  hgvsp: ENST00000554966.1:c.909G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.660G>T
  hgvsp: ENST00000553879.1:c.660G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.834G>T
  hgvsp: ENST00000555453.1:c.834G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1059G>T
  hgvsp: ENST00000554591.1:c.1059G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.870G>T
  hgvsp: ENST00000554050.1:c.870G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.660G>T
  hgvsp: ENST00000554661.1:c.660G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.870G>T
  hgvsp: ENST00000553708.1:c.870G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.966G>T
  hgvsp: ENST00000539237.2:c.966G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.909G>T
  hgvsp: ENST00000424781.2:c.909G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.966G>T
  hgvsp: ENST00000556279.1:c.966G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.834G>T
  hgvsp: ENST00000556169.1:c.834G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.870G>T
  hgvsp: ENST00000250373.4:c.870G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.660G>T
  hgvsp: ENST00000554344.1:c.660G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+598G>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1070G>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.909G>T
  hgvsp: ENST00000555590.1:c.909G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.660G>T
  hgvsp: ENST00000557451.1:c.660G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.966G>T
  hgvsp: ENST00000553469.1:c.966G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1059G>T
  hgvsp: ENST00000413692.2:c.1059G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu353Leu
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

14-24839487-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839487
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839487
    reference: chr 14
allele count: 1
allele frequency: 8.621878879845495e-6
allele num: 115984
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.979T>A
  hgvsp: ENSP00000451502.1:p.Ser327Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.883T>A
  hgvsp: ENSP00000450590.1:p.Ser295Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.883T>A
  hgvsp: ENSP00000250373.4:p.Ser295Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.882T>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.922T>A
  hgvsp: ENSP00000450644.1:p.Ser308Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.922T>A
  hgvsp: ENSP00000388668.2:p.Ser308Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.673T>A
  hgvsp: ENSP00000450469.1:p.Ser225Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1083T>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.1004T>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.979T>A
  hgvsp: ENSP00000452270.1:p.Ser327Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1176T>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.883T>A
  hgvsp: ENSP00000451151.1:p.Ser295Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.847T>A
  hgvsp: ENSP00000451454.1:p.Ser283Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1072T>A
  hgvsp: ENSP00000452039.1:p.Ser358Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.847T>A
  hgvsp: ENSP00000396788.3:p.Ser283Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.922T>A
  hgvsp: ENSP00000451224.1:p.Ser308Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+611T>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.673T>A
  hgvsp: ENSP00000451284.1:p.Ser225Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1072T>A
  hgvsp: ENSP00000388910.2:p.Ser358Thr
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+611T>A
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser358Thr
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-24839497-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839497
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839497
    reference: chr 14
allele count: 1
allele frequency: 8.597121683660311e-6
allele num: 116318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.893C>T
  hgvsp: ENSP00000250373.4:p.Pro298Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.1014C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.989C>T
  hgvsp: ENSP00000452270.1:p.Pro330Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.683C>T
  hgvsp: ENSP00000450469.1:p.Pro228Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1082C>T
  hgvsp: ENSP00000452039.1:p.Pro361Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.932C>T
  hgvsp: ENSP00000388668.2:p.Pro311Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.857C>T
  hgvsp: ENSP00000396788.3:p.Pro286Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.893C>T
  hgvsp: ENSP00000451151.1:p.Pro298Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1093C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.857C>T
  hgvsp: ENSP00000450686.1:p.Pro286Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1082C>T
  hgvsp: ENSP00000388910.2:p.Pro361Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.683C>T
  hgvsp: ENSP00000451284.1:p.Pro228Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.932C>T
  hgvsp: ENSP00000451224.1:p.Pro311Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.683C>T
  hgvsp: ENSP00000452349.1:p.Pro228Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.857C>T
  hgvsp: ENSP00000451454.1:p.Pro286Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.893C>T
  hgvsp: ENSP00000450590.1:p.Pro298Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.989C>T
  hgvsp: ENSP00000439350.2:p.Pro330Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.989C>T
  hgvsp: ENSP00000451502.1:p.Pro330Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+621C>T
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro361Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

14-24839499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839499
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839499
    reference: chr 14
allele count: 12
allele frequency: 1.0316191262186e-4
allele num: 116322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.859C>T
  hgvsp: ENSP00000451454.1:p.Pro287Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.991C>T
  hgvsp: ENSP00000452270.1:p.Pro331Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1188C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.685C>T
  hgvsp: ENSP00000451284.1:p.Pro229Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.685C>T
  hgvsp: ENSP00000450733.1:p.Pro229Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.934C>T
  hgvsp: ENSP00000388668.2:p.Pro312Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1084C>T
  hgvsp: ENSP00000452039.1:p.Pro362Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.1016C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.895C>T
  hgvsp: ENSP00000450590.1:p.Pro299Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.859C>T
  hgvsp: ENSP00000396788.3:p.Pro287Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.685C>T
  hgvsp: ENSP00000450469.1:p.Pro229Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.895C>T
  hgvsp: ENSP00000250373.4:p.Pro299Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.934C>T
  hgvsp: ENSP00000450644.1:p.Pro312Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.685C>T
  hgvsp: ENSP00000452349.1:p.Pro229Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.895C>T
  hgvsp: ENSP00000451151.1:p.Pro299Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.859C>T
  hgvsp: ENSP00000450686.1:p.Pro287Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.991C>T
  hgvsp: ENSP00000451502.1:p.Pro331Ser
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.894C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+623C>T
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro362Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

14-24839507-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839507
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839507
    reference: chr 14
allele count: 1
allele frequency: 8.584133088399403e-6
allele num: 116494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.867C>T
  hgvsp: ENST00000422617.3:c.867C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.693C>T
  hgvsp: ENST00000554344.1:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1092C>T
  hgvsp: ENST00000554591.1:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.693C>T
  hgvsp: ENST00000553879.1:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.999C>T
  hgvsp: ENST00000556279.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1196C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.903C>T
  hgvsp: ENST00000250373.4:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.942C>T
  hgvsp: ENST00000555590.1:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.1024C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.942C>T
  hgvsp: ENST00000424781.2:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1103C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.942C>T
  hgvsp: ENST00000554966.1:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+631C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.999C>T
  hgvsp: ENST00000539237.2:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.903C>T
  hgvsp: ENST00000554050.1:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.867C>T
  hgvsp: ENST00000556169.1:c.867C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.999C>T
  hgvsp: ENST00000553469.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+631C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.903C>T
  hgvsp: ENST00000553708.1:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.902C>T
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro364Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

14-24839508-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839508
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839508
    reference: chr 14
allele count: 1
allele frequency: 8.580155815629612e-6
allele num: 116548
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.1025C>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.904C>G
  hgvsp: ENSP00000250373.4:p.Pro302Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.694C>G
  hgvsp: ENSP00000450469.1:p.Pro232Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.904C>G
  hgvsp: ENSP00000450590.1:p.Pro302Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.904C>G
  hgvsp: ENSP00000451151.1:p.Pro302Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.868C>G
  hgvsp: ENSP00000451454.1:p.Pro290Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.694C>G
  hgvsp: ENSP00000452349.1:p.Pro232Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.1000C>G
  hgvsp: ENSP00000451502.1:p.Pro334Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.694C>G
  hgvsp: ENSP00000451284.1:p.Pro232Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.868C>G
  hgvsp: ENSP00000396788.3:p.Pro290Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.943C>G
  hgvsp: ENSP00000450644.1:p.Pro315Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1093C>G
  hgvsp: ENSP00000452039.1:p.Pro365Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.694C>G
  hgvsp: ENSP00000450733.1:p.Pro232Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.943C>G
  hgvsp: ENSP00000451224.1:p.Pro315Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.903C>G
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.1000C>G
  hgvsp: ENSP00000452270.1:p.Pro334Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000439350
  ensembl transcript: ENST00000539237
  gene symbol: NFATC4
  hgvsc: ENST00000539237.2:c.1000C>G
  hgvsp: ENSP00000439350.2:p.Pro334Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.943C>G
  hgvsp: ENSP00000388668.2:p.Pro315Ala
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1104C>G
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro365Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum

14-24839515-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839515
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839515
    reference: chr 14
allele count: 3
allele frequency: 2.573870071038814e-5
allele num: 116556
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.950C>T
  hgvsp: ENSP00000388668.2:p.Pro317Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.875C>T
  hgvsp: ENSP00000451454.1:p.Pro292Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.875C>T
  hgvsp: ENSP00000396788.3:p.Pro292Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.911C>T
  hgvsp: ENSP00000450590.1:p.Pro304Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.911C>T
  hgvsp: ENSP00000451151.1:p.Pro304Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.1007C>T
  hgvsp: ENSP00000452270.1:p.Pro336Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.910C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1100C>T
  hgvsp: ENSP00000452039.1:p.Pro367Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.911C>T
  hgvsp: ENSP00000250373.4:p.Pro304Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450686
  ensembl transcript: ENST00000555453
  gene symbol: NFATC4
  hgvsc: ENST00000555453.1:c.875C>T
  hgvsp: ENSP00000450686.1:p.Pro292Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.1007C>T
  hgvsp: ENSP00000451502.1:p.Pro336Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.701C>T
  hgvsp: ENSP00000450733.1:p.Pro234Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.950C>T
  hgvsp: ENSP00000451224.1:p.Pro317Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1100C>T
  hgvsp: ENSP00000388910.2:p.Pro367Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.701C>T
  hgvsp: ENSP00000450469.1:p.Pro234Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1204C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.950C>T
  hgvsp: ENSP00000450644.1:p.Pro317Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.701C>T
  hgvsp: ENSP00000451284.1:p.Pro234Leu
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.701C>T
  hgvsp: ENSP00000452349.1:p.Pro234Leu
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro367Leu
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

14-24839521-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839521
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839521
    reference: chr 14
allele count: 1
allele frequency: 8.59136052785319e-6
allele num: 116396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.917C>T
  hgvsp: ENSP00000250373.4:p.Ala306Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556957
  gene symbol: NFATC4
  hgvsc: ENST00000556957.1:n.1038C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.707C>T
  hgvsp: ENSP00000452349.1:p.Ala236Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.916C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+645C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.956C>T
  hgvsp: ENSP00000450644.1:p.Ala319Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.1013C>T
  hgvsp: ENSP00000452270.1:p.Ala338Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.956C>T
  hgvsp: ENSP00000388668.2:p.Ala319Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+645C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.881C>T
  hgvsp: ENSP00000451454.1:p.Ala294Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450733
  ensembl transcript: ENST00000554661
  gene symbol: NFATC4
  hgvsc: ENST00000554661.1:c.707C>T
  hgvsp: ENSP00000450733.1:p.Ala236Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.917C>T
  hgvsp: ENSP00000451151.1:p.Ala306Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1117C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.707C>T
  hgvsp: ENSP00000450469.1:p.Ala236Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.917C>T
  hgvsp: ENSP00000450590.1:p.Ala306Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000554655
  gene symbol: NFATC4
  hgvsc: ENST00000554655.1:n.1210C>T
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.956C>T
  hgvsp: ENSP00000451224.1:p.Ala319Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.707C>T
  hgvsp: ENSP00000451284.1:p.Ala236Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.881C>T
  hgvsp: ENSP00000396788.3:p.Ala294Val
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1106C>T
  hgvsp: ENSP00000388910.2:p.Ala369Val
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala369Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

14-24839524-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24839524
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24839524
    reference: chr 14
allele count: 2
allele frequency: 1.715148188803513e-5
allele num: 116608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452039
  ensembl transcript: ENST00000554591
  gene symbol: NFATC4
  hgvsc: ENST00000554591.1:c.1109G>A
  hgvsp: ENSP00000452039.1:p.Arg370Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388668
  ensembl transcript: ENST00000424781
  gene symbol: NFATC4
  hgvsc: ENST00000424781.2:c.959G>A
  hgvsp: ENSP00000388668.2:p.Arg320Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000396788
  ensembl transcript: ENST00000422617
  gene symbol: NFATC4
  hgvsc: ENST00000422617.3:c.884G>A
  hgvsp: ENSP00000396788.3:p.Arg295Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450590
  ensembl transcript: ENST00000553708
  gene symbol: NFATC4
  hgvsc: ENST00000553708.1:c.920G>A
  hgvsp: ENSP00000450590.1:p.Arg307Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451502
  ensembl transcript: ENST00000553469
  gene symbol: NFATC4
  hgvsc: ENST00000553469.1:c.1016G>A
  hgvsp: ENSP00000451502.1:p.Arg339Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451151
  ensembl transcript: ENST00000554050
  gene symbol: NFATC4
  hgvsc: ENST00000554050.1:c.920G>A
  hgvsp: ENSP00000451151.1:p.Arg307Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452270
  ensembl transcript: ENST00000556279
  gene symbol: NFATC4
  hgvsc: ENST00000556279.1:c.1016G>A
  hgvsp: ENSP00000452270.1:p.Arg339Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450644
  ensembl transcript: ENST00000554966
  gene symbol: NFATC4
  hgvsc: ENST00000554966.1:c.959G>A
  hgvsp: ENSP00000450644.1:p.Arg320Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000450469
  ensembl transcript: ENST00000554344
  gene symbol: NFATC4
  hgvsc: ENST00000554344.1:c.710G>A
  hgvsp: ENSP00000450469.1:p.Arg237Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451454
  ensembl transcript: ENST00000556169
  gene symbol: NFATC4
  hgvsc: ENST00000556169.1:c.884G>A
  hgvsp: ENSP00000451454.1:p.Arg295Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000388910
  ensembl transcript: ENST00000413692
  gene symbol: NFATC4
  hgvsc: ENST00000413692.2:c.1109G>A
  hgvsp: ENSP00000388910.2:p.Arg370Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451224
  ensembl transcript: ENST00000555590
  gene symbol: NFATC4
  hgvsc: ENST00000555590.1:c.959G>A
  hgvsp: ENSP00000451224.1:p.Arg320Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000452349
  ensembl transcript: ENST00000553879
  gene symbol: NFATC4
  hgvsc: ENST00000553879.1:c.710G>A
  hgvsp: ENSP00000452349.1:p.Arg237Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000556302
  gene symbol: NFATC4
  hgvsc: ENST00000556302.1:n.919G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000440487
  gene symbol: NFATC4
  hgvsc: ENST00000440487.2:n.1120G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000250373
  ensembl transcript: ENST00000250373
  gene symbol: NFATC4
  hgvsc: ENST00000250373.4:c.920G>A
  hgvsp: ENSP00000250373.4:p.Arg307Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451284
  ensembl transcript: ENST00000557451
  gene symbol: NFATC4
  hgvsc: ENST00000557451.1:c.710G>A
  hgvsp: ENSP00000451284.1:p.Arg237Gln
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl transcript: ENST00000557028
  gene symbol: NFATC4
  hgvsc: ENST00000557028.1:n.427+648G>A
  variant of: http://identifiers.org/hgnc/7778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100968
  ensembl protein: ENSP00000451992
  ensembl transcript: ENST00000554779
  gene symbol: NFATC4
  hgvsc: ENST00000554779.1:c.272+648G>A
  variant of: http://identifiers.org/hgnc/7778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
hgvs: p.Arg370Gln
num of homozygotes: 0
reference allele: G

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.420C>A
hgvsp: ENST00000554661.1:c.420C>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451454
ensembl transcript: ENST00000556169
gene symbol: NFATC4
hgvsc: ENST00000556169.1:c.594C>A
hgvsp: ENST00000556169.1:c.594C>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.630C>A
hgvsp: ENST00000553708.1:c.630C>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.751C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.923C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+358C>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 15926
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1195
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 23529
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2246
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 326
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9758
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2112
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2715
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1547
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2947
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9229
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32359
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3269
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2872
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.204717343930265e-5
allele num: 62408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6234
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

DP
type: SiteQuality
SIO_000300: 1.540671e6

MQRankSum
type: SiteQuality
SIO_000300: 6.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.347e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.22e-1

QD
type: SiteQuality
SIO_000300: 1.194e1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.892e0

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.830C>T
hgvsp: ENSP00000388910.2:p.Pro277Leu
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.737C>T
hgvsp: ENSP00000451502.1:p.Pro246Leu
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.762C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.431C>T
hgvsp: ENSP00000451284.1:p.Pro144Leu
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000452270
ensembl transcript: ENST00000556279
gene symbol: NFATC4
hgvsc: ENST00000556279.1:c.737C>T
hgvsp: ENSP00000452270.1:p.Pro246Leu
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+369C>T
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 2239
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16002
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1265
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2443
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2672
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9504
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 923
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23130
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1749
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 325
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3013
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31783
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1624
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3211
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2822
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9054
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.118453255017132e-5
allele num: 16344
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.255e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

DP
type: SiteQuality
SIO_000300: 1.528317e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.02e1

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.831G>A
hgvsp: ENST00000413692.2:c.831G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.935G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.738G>A
hgvsp: ENST00000553469.1:c.738G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.763G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000396788
ensembl transcript: ENST00000422617
gene symbol: NFATC4
hgvsc: ENST00000422617.3:c.606G>A
hgvsp: ENST00000422617.3:c.606G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.641G>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 16057
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2657
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 922
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2435
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2252
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1263
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 23137
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1736
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9476
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32151
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2803
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6180
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62136
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

DP
type: SiteQuality
SIO_000300: 1.528105e6

QD
type: SiteQuality
SIO_000300: 1.062e1

MQ
type: SiteQuality
SIO_000300: 5.925e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.691e0

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

FS
type: SiteQuality
SIO_000300: 2.448e0

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451151
ensembl transcript: ENST00000554050
gene symbol: NFATC4
hgvsc: ENST00000554050.1:c.642G>T
hgvsp: ENST00000554050.1:c.642G>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.738G>T
hgvsp: ENST00000539237.2:c.738G>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.763G>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.606G>T
hgvsp: ENST00000555453.1:c.606G>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.432G>T
hgvsp: ENST00000554661.1:c.432G>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 1736
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2252
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23137
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2435
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2657
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1263
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 320
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9476
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16057
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 922
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1349
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32151
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2803
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62136
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.768033946251768e-4
allele num: 11312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6180
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.55e-1

QD
type: SiteQuality
SIO_000300: 1.062e1

FS
type: SiteQuality
SIO_000300: 2.448e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.691e0

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 1.528105e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.24e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.645G>A
hgvsp: ENST00000553708.1:c.645G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000452352
ensembl transcript: ENST00000557674
gene symbol: NFATC4
hgvsc: ENST00000557674.1:c.576G>A
hgvsp: ENST00000557674.1:c.576G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450644
ensembl transcript: ENST00000554966
gene symbol: NFATC4
hgvsc: ENST00000554966.1:c.684G>A
hgvsp: ENST00000554966.1:c.684G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+373G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000396788
ensembl transcript: ENST00000422617
gene symbol: NFATC4
hgvsc: ENST00000422617.3:c.609G>A
hgvsp: ENST00000422617.3:c.609G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+373G>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 912
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16161
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2272
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 23087
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2493
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1267
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9402
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2648
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1690
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32567
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9067
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3204
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1174
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2797
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62164
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.011e0

QD
type: SiteQuality
SIO_000300: 1.25e0

VQSLOD
type: SiteQuality
SIO_000300: -3.239e0

DP
type: SiteQuality
SIO_000300: 1.525676e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.65e-1

FS
type: SiteQuality
SIO_000300: 1.075e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.949G>C
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.752G>C
hgvsp: ENSP00000439350.2:p.Arg251Pro
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000396788
ensembl transcript: ENST00000422617
gene symbol: NFATC4
hgvsc: ENST00000422617.3:c.620G>C
hgvsp: ENSP00000396788.3:p.Arg207Pro
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.446G>C
hgvsp: ENSP00000451284.1:p.Arg149Pro
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.656G>C
hgvsp: ENSP00000450590.1:p.Arg219Pro
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 2404
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2727
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22769
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9233
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16196
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1308
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 894
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1786
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2612
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 951
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3406
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3133
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32378
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8883
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.614726303891491e-5
allele num: 61930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6132
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.606e0

QD
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.738e1

VQSLOD
type: SiteQuality
SIO_000300: -2.334e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

DP
type: SiteQuality
SIO_000300: 1.515578e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.54e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.447G>A
hgvsp: ENST00000554661.1:c.447G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.447G>A
hgvsp: ENST00000557451.1:c.447G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.846G>A
hgvsp: ENST00000413692.2:c.846G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.778G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.753G>A
hgvsp: ENST00000553469.1:c.753G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 1308
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16234
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 891
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2741
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9179
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1790
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2432
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22764
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2596
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3149
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1352
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3463
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8905
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32473
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 645
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1590
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16334
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61972
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.844861135680169e-5
allele num: 11306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6138
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.514148e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 1.163e1

MQRankSum
type: SiteQuality
SIO_000300: -3.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.059e0

FS
type: SiteQuality
SIO_000300: 1.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.624C>A
hgvsp: ENST00000555453.1:c.624C>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.781C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000396788
ensembl transcript: ENST00000422617
gene symbol: NFATC4
hgvsc: ENST00000422617.3:c.624C>A
hgvsp: ENST00000422617.3:c.624C>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.659C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+388C>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 9136
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1304
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16163
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2843
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1951
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2498
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 887
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 306
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22564
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2588
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31700
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3142
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2743
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8822
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.615978798358166e-5
allele num: 61882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.52e-1

MQ
type: SiteQuality
SIO_000300: 5.902e1

DP
type: SiteQuality
SIO_000300: 1.509693e6

FS
type: SiteQuality
SIO_000300: 3.782e0

QD
type: SiteQuality
SIO_000300: 1.463e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.13e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.68e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451454
ensembl transcript: ENST00000556169
gene symbol: NFATC4
hgvsc: ENST00000556169.1:c.624C>T
hgvsp: ENST00000556169.1:c.624C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.860C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+388C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388668
ensembl transcript: ENST00000424781
gene symbol: NFATC4
hgvsc: ENST00000424781.2:c.699C>T
hgvsp: ENST00000424781.2:c.699C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.849C>T
hgvsp: ENST00000413692.2:c.849C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 2498
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2588
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 306
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 887
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1304
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22564
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16163
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2843
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1951
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9136
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 234
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8822
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3142
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31700
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.615978798358166e-5
allele num: 61882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQ
type: SiteQuality
SIO_000300: 5.902e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.13e-2

DP
type: SiteQuality
SIO_000300: 1.509693e6

FS
type: SiteQuality
SIO_000300: 3.782e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.463e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+394T>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.959T>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.456T>G
hgvsp: ENST00000554661.1:c.456T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.855T>G
hgvsp: ENST00000413692.2:c.855T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.666T>G
hgvsp: ENST00000553708.1:c.666T>G(p.%3D)
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1967
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 304
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2922
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9002
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2568
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16311
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2571
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1294
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22437
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 878
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1027
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1566
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3671
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8792
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31868
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.344665885111372e-4
allele num: 8530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61814
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8290
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.39e-1

DP
type: SiteQuality
SIO_000300: 1.506055e6

MQRankSum
type: SiteQuality
SIO_000300: -3.94e-1

FS
type: SiteQuality
SIO_000300: 2.671e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

QD
type: SiteQuality
SIO_000300: 1.443e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000396788
ensembl transcript: ENST00000422617
gene symbol: NFATC4
hgvsc: ENST00000422617.3:c.631C>T
hgvsp: ENSP00000396788.3:p.Arg211Trp
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.631C>T
hgvsp: ENSP00000450686.1:p.Arg211Trp
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.960C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388668
ensembl transcript: ENST00000424781
gene symbol: NFATC4
hgvsc: ENST00000424781.2:c.706C>T
hgvsp: ENSP00000388668.2:p.Arg236Trp
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.867C>T
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 27
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9011
bin: 3.25e1
variant carriers: 6

GenotypeDepth
all individuals: 1984
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 313
bin: 4.75e1
variant carriers: 8

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 115
bin: 5.25e1
variant carriers: 5

GenotypeDepth
all individuals: 2582
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1282
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 878
bin: 4.25e1
variant carriers: 4

GenotypeDepth
all individuals: 25
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2957
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2578
bin: 3.75e1
variant carriers: 8

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 16292
bin: 2.25e1
variant carriers: 3

GenotypeDepth
all individuals: 22371
bin: 2.75e1
variant carriers: 6

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1552
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3081
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31634
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8740
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2669
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 9.75e1
variant carriers: 48

GenotypeQuality
all individuals: 1009
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3708
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.515381786983699e-4
allele num: 16318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.541703559412077e-4
allele num: 11294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 4.696964788960513e-4
allele num: 61742
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.207729468599034e-4
allele num: 8280
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.853430110044487e-4
allele num: 8542
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

DP
type: SiteQuality
SIO_000300: 1.505936e6

QD
type: SiteQuality
SIO_000300: 1.256e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.877C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.970C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000396788
ensembl transcript: ENST00000422617
gene symbol: NFATC4
hgvsc: ENST00000422617.3:c.641C>A
hgvsp: ENSP00000396788.3:p.Thr214Asn
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.467C>A
hgvsp: ENSP00000450733.1:p.Thr156Asn
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+405C>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 2539
bin: 3.75e1
variant carriers: 24

GenotypeDepth
all individuals: 6
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 2741
bin: 7.5e0
variant carriers: 4

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.75e1
variant carriers: 7

GenotypeDepth
all individuals: 1154
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 300
bin: 4.75e1
variant carriers: 9

GenotypeDepth
all individuals: 59
bin: 5.75e1
variant carriers: 8

GenotypeDepth
all individuals: 876
bin: 4.25e1
variant carriers: 16

GenotypeDepth
all individuals: 3152
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16428
bin: 2.25e1
variant carriers: 10

GenotypeDepth
all individuals: 30
bin: 7.25e1
variant carriers: 8

GenotypeDepth
all individuals: 1929
bin: 1.75e1
variant carriers: 7

GenotypeDepth
all individuals: 22327
bin: 2.75e1
variant carriers: 25

GenotypeDepth
all individuals: 120
bin: 5.25e1
variant carriers: 14

GenotypeDepth
all individuals: 36
bin: 6.25e1
variant carriers: 5

GenotypeDepth
all individuals: 18
bin: 7.75e1
variant carriers: 4

GenotypeDepth
all individuals: 8815
bin: 3.25e1
variant carriers: 12

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8620
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1530
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4121
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 362
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 185
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1055
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 9.75e1
variant carriers: 154

GenotypeQuality
all individuals: 3004
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32279
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 173
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 143
allele frequency: 8.773006134969326e-3
allele num: 16300
num of homozygotes: 1

Latino
type: Population
allele count: 1
allele frequency: 8.854258898530193e-5
allele num: 11294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8282
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6078
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.685503685503686e-3
allele num: 814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.854054753737622e-5
allele num: 61804
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.818012566907144e-4
allele num: 8594
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.2e1

DP
type: SiteQuality
SIO_000300: 1.502955e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.805e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-2

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.646G>A
hgvsp: ENSP00000450686.1:p.Glu216Lys
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.472G>A
hgvsp: ENSP00000450733.1:p.Glu158Lys
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000250373
ensembl transcript: ENST00000250373
gene symbol: NFATC4
hgvsc: ENST00000250373.4:c.682G>A
hgvsp: ENSP00000250373.4:p.Glu228Lys
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+410G>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2510
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2072
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8786
bin: 3.25e1
variant carriers: 3

GenotypeDepth
all individuals: 16356
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3346
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2811
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22181
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1117
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 851
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 610
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1510
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4223
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2574
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8483
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31866
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2986
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 9.75e1
variant carriers: 8

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61712
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16300
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 7.0859167404783e-4
allele num: 11290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.495923e6

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

FS
type: SiteQuality
SIO_000300: 3.08e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.199e1

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.877C>T
hgvsp: ENSP00000388910.2:p.Pro293Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.809C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.687C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+416C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.478C>T
hgvsp: ENSP00000451284.1:p.Pro160Ser
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 16275
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8685
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2488
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1065
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2882
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 843
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2185
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3497
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22127
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8456
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4463
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2951
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1089
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2569
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32020
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11288
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.227596366314756e-4
allele num: 16292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.619170984455958e-5
allele num: 61760
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.493e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.005e0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 1.492141e6

FS
type: SiteQuality
SIO_000300: 1.2315e1

QD
type: SiteQuality
SIO_000300: 1.417e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.57e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.816G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.895G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451151
ensembl transcript: ENST00000554050
gene symbol: NFATC4
hgvsc: ENST00000554050.1:c.695G>A
hgvsp: ENSP00000451151.1:p.Ser232Asn
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.485G>A
hgvsp: ENSP00000450733.1:p.Ser162Asn
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+423G>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3843
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2455
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 286
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16098
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2987
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 993
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 835
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2513
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21802
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8531
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4807
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31434
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1473
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8323
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2505
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 598
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8670
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6022
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.620693008330362e-5
allele num: 61702
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.02e-1

DP
type: SiteQuality
SIO_000300: 1.483257e6

FS
type: SiteQuality
SIO_000300: 4.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.025e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450644
ensembl transcript: ENST00000554966
gene symbol: NFATC4
hgvsc: ENST00000554966.1:c.735C>G
hgvsp: ENSP00000450644.1:p.Ser245Arg
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451454
ensembl transcript: ENST00000556169
gene symbol: NFATC4
hgvsc: ENST00000556169.1:c.660C>G
hgvsp: ENSP00000451454.1:p.Ser220Arg
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000250373
ensembl transcript: ENST00000250373
gene symbol: NFATC4
hgvsc: ENST00000250373.4:c.696C>G
hgvsp: ENSP00000250373.4:p.Ser232Arg
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.486C>G
hgvsp: ENSP00000450733.1:p.Ser162Arg
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 836
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 285
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2996
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2770
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1003
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21653
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8490
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2455
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 15861
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3996
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8228
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 670
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2488
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30345
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2880
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4780
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.155001155001155e-4
allele num: 8658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6018
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

FS
type: SiteQuality
SIO_000300: 1.095e0

QD
type: SiteQuality
SIO_000300: 1.337e1

DP
type: SiteQuality
SIO_000300: 1.478931e6

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.699G>C
hgvsp: ENST00000553708.1:c.699G>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.663G>C
hgvsp: ENST00000555453.1:c.663G>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451224
ensembl transcript: ENST00000555590
gene symbol: NFATC4
hgvsc: ENST00000555590.1:c.738G>C
hgvsp: ENST00000555590.1:c.738G>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.698G>C
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4038
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3022
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8436
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 21577
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15959
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 835
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 975
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2450
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2771
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 286
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4905
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31056
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8128
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1397
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2821
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2447
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61698
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8264
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.552397868561279e-4
allele num: 11260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8676
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

FS
type: SiteQuality
SIO_000300: 7.33e0

DP
type: SiteQuality
SIO_000300: 1.477854e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: 3.19e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

QD
type: SiteQuality
SIO_000300: 1.35e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450644
ensembl transcript: ENST00000554966
gene symbol: NFATC4
hgvsc: ENST00000554966.1:c.741T>C
hgvsp: ENST00000554966.1:c.741T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451151
ensembl transcript: ENST00000554050
gene symbol: NFATC4
hgvsc: ENST00000554050.1:c.702T>C
hgvsp: ENST00000554050.1:c.702T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+430T>C
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.701T>C
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451454
ensembl transcript: ENST00000556169
gene symbol: NFATC4
hgvsc: ENST00000556169.1:c.666T>C
hgvsp: ENST00000556169.1:c.666T>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21376
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3072
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4195
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8338
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 955
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3084
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2429
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15793
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 825
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2443
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8109
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1498
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30571
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5060
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1068
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5996
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8698
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.621323648626739e-5
allele num: 61678
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.617e0

MQRankSum
type: SiteQuality
SIO_000300: -2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.211e0

QD
type: SiteQuality
SIO_000300: 1.03e1

MQ
type: SiteQuality
SIO_000300: 5.881e1

FS
type: SiteQuality
SIO_000300: 4.368e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

DP
type: SiteQuality
SIO_000300: 1.471598e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.832C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.675C>A
hgvsp: ENSP00000450686.1:p.Ser225Arg
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.710C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+439C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.807C>A
hgvsp: ENSP00000451502.1:p.Ser269Arg
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 817
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 964
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8034
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3190
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20263
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15087
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4591
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4727
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 285
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2403
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2365
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5166
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7596
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2709
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1803
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1943
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27159
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1680
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 885
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.627551186484815e-5
allele num: 61442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5942
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.949e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

DP
type: SiteQuality
SIO_000300: 1.448442e6

FS
type: SiteQuality
SIO_000300: 4.981e0

VQSLOD
type: SiteQuality
SIO_000300: -7.118e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.017e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.86e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

QD
type: SiteQuality
SIO_000300: 1.089e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.504C>T
hgvsp: ENST00000554661.1:c.504C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+442C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.903C>T
hgvsp: ENST00000413692.2:c.903C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451224
ensembl transcript: ENST00000555590
gene symbol: NFATC4
hgvsc: ENST00000555590.1:c.753C>T
hgvsp: ENST00000555590.1:c.753C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.835C>T
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 4720
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 952
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3216
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2395
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19998
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4778
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 818
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15318
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7891
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1833
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27679
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1711
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1007
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5264
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2671
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16212
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.21153380179307e-4
allele num: 8254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.628664495114006e-5
allele num: 61400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5932
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.539e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.57e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

DP
type: SiteQuality
SIO_000300: 1.444482e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.41e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1015G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.722G>A
hgvsp: ENSP00000450590.1:p.Arg241Gln
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.512G>A
hgvsp: ENSP00000451284.1:p.Arg171Gln
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.721G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.818G>A
hgvsp: ENSP00000439350.2:p.Arg273Gln
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 811
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5290
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3312
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5014
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2338
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 278
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18823
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 7531
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 897
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16088
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2623
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1981
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5581
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1590
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26051
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1059
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1413
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7268
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.629142093773419e-5
allele num: 61382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.21153380179307e-4
allele num: 8254
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.850000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

QD
type: SiteQuality
SIO_000300: 1.072e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.428824e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.856T>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.831T>G
hgvsp: ENSP00000451502.1:p.Asp277Glu
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.699T>G
hgvsp: ENSP00000450686.1:p.Asp233Glu
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.935T>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.734T>G
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 5455
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5167
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7310
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18226
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 795
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 277
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16604
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2316
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 821
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3418
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27574
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2072
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5952
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7219
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1095
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1286
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2618
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5884
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 1.421114e6

FS
type: SiteQuality
SIO_000300: 6.854e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

QD
type: SiteQuality
SIO_000300: 1.173e1

VQSLOD
type: SiteQuality
SIO_000300: 4.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.76e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.937G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000250373
ensembl transcript: ENST00000250373
gene symbol: NFATC4
hgvsc: ENST00000250373.4:c.737G>A
hgvsp: ENSP00000250373.4:p.Ser246Asn
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.736G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.833G>A
hgvsp: ENSP00000439350.2:p.Ser278Asn
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+465G>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 5209
bin: 1.25e1
variant carriers: 16

GenotypeDepth
all individuals: 18038
bin: 2.75e1
variant carriers: 22

GenotypeDepth
all individuals: 31
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3414
bin: 7.5e0
variant carriers: 7

GenotypeDepth
all individuals: 7325
bin: 3.25e1
variant carriers: 19

GenotypeDepth
all individuals: 2330
bin: 3.75e1
variant carriers: 11

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 798
bin: 4.25e1
variant carriers: 6

GenotypeDepth
all individuals: 284
bin: 4.75e1
variant carriers: 6

GenotypeDepth
all individuals: 16506
bin: 2.25e1
variant carriers: 20

GenotypeDepth
all individuals: 6
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 820
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5665
bin: 1.75e1
variant carriers: 19

GenotypeQuality
all individuals: 890
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7165
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 79
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27067
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2573
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2264
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1921
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 9.75e1
variant carriers: 123

GenotypeQuality
all individuals: 315
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1394
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 5919
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1387
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2268
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 119
allele frequency: 1.36593204775023e-2
allele num: 8712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16220
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.573981415296641e-4
allele num: 11192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61416
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e-1

FS
type: SiteQuality
SIO_000300: 5.2e-1

QD
type: SiteQuality
SIO_000300: 1.327e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.571e0

DP
type: SiteQuality
SIO_000300: 1.419464e6

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.931C>T
hgvsp: ENST00000413692.2:c.931C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.838C>T
hgvsp: ENST00000553469.1:c.838C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000452349
ensembl transcript: ENST00000553879
gene symbol: NFATC4
hgvsc: ENST00000553879.1:c.532C>T
hgvsp: ENST00000553879.1:c.532C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388668
ensembl transcript: ENST00000424781
gene symbol: NFATC4
hgvsc: ENST00000424781.2:c.781C>T
hgvsp: ENST00000424781.2:c.781C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 2308
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3401
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 17835
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 874
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7308
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16357
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5258
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 279
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5969
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 800
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2028
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2269
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5952
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26487
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2199
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2583
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2392
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7167
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5840
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.628823663550184e-5
allele num: 61394
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.934953538241601e-5
allele num: 11192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.69e-1

FS
type: SiteQuality
SIO_000300: 4.032e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-1

DP
type: SiteQuality
SIO_000300: 1.414764e6

QD
type: SiteQuality
SIO_000300: 1.349e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.402e0

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.846C>T
hgvsp: ENST00000553469.1:c.846C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+478C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451454
ensembl transcript: ENST00000556169
gene symbol: NFATC4
hgvsc: ENST00000556169.1:c.714C>T
hgvsp: ENST00000556169.1:c.714C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+478C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.939C>T
hgvsp: ENST00000413692.2:c.939C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 5134
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7262
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17527
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3462
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 279
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5901
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16831
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 884
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2314
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27059
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2569
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6885
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 986
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2265
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5846
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2173
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 262
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8244
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5816
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.7e0

DP
type: SiteQuality
SIO_000300: 1.413048e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.675e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.295e0

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.860C>T
hgvsp: ENSP00000439350.2:p.Pro287Leu
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.953C>T
hgvsp: ENSP00000388910.2:p.Pro318Leu
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.860C>T
hgvsp: ENSP00000451502.1:p.Pro287Leu
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.554C>T
hgvsp: ENSP00000451284.1:p.Pro185Leu
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5097
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 946
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3317
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 795
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 280
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17727
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17678
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2308
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4839
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7387
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5225
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2265
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2020
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7355
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1462
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27493
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1067
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1090
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.630470227613644e-5
allele num: 61332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16222
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

DP
type: SiteQuality
SIO_000300: 1.422146e6

FS
type: SiteQuality
SIO_000300: 1.808e0

MQRankSum
type: SiteQuality
SIO_000300: -3.91e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.939e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.04e-1

MQ
type: SiteQuality
SIO_000300: 5.829e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+497C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451151
ensembl transcript: ENST00000554050
gene symbol: NFATC4
hgvsc: ENST00000554050.1:c.769C>T
hgvsp: ENSP00000451151.1:p.Pro257Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.865C>T
hgvsp: ENSP00000439350.2:p.Pro289Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.768C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1062C>T
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 18490
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3210
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4629
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17365
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2386
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4562
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 925
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7690
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 810
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4923
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2518
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27910
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2061
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1214
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.904719501335708e-5
allele num: 11230
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.205400192864031e-4
allele num: 8296
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.627180421765165e-5
allele num: 61456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16234
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.05e-1

DP
type: SiteQuality
SIO_000300: 1.437626e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.437e0

VQSLOD
type: SiteQuality
SIO_000300: -2.054e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.868e0

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

QD
type: SiteQuality
SIO_000300: 1.331e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+501C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1066C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+501C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451151
ensembl transcript: ENST00000554050
gene symbol: NFATC4
hgvsc: ENST00000554050.1:c.773C>T
hgvsp: ENSP00000451151.1:p.Ala258Val
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.962C>T
hgvsp: ENSP00000388910.2:p.Ala321Val
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 17799
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3210
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7796
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 287
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 914
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4024
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18704
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 805
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2393
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4423
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1531
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4763
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2557
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28474
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7562
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1881
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2864
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.625434803810019e-5
allele num: 61522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5886
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

QD
type: SiteQuality
SIO_000300: 8.58e0

DP
type: SiteQuality
SIO_000300: 1.444543e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.182e-1

FS
type: SiteQuality
SIO_000300: 7.969e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.871e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.19e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000250373
ensembl transcript: ENST00000250373
gene symbol: NFATC4
hgvsc: ENST00000250373.4:c.779C>A
hgvsp: ENSP00000250373.4:p.Pro260Gln
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451454
ensembl transcript: ENST00000556169
gene symbol: NFATC4
hgvsc: ENST00000556169.1:c.743C>A
hgvsp: ENSP00000451454.1:p.Pro248Gln
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000396788
ensembl transcript: ENST00000422617
gene symbol: NFATC4
hgvsc: ENST00000422617.3:c.743C>A
hgvsp: ENSP00000396788.3:p.Pro248Gln
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.900C>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 3191
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 870
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 287
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4076
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7996
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19301
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2437
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3258
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18135
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 813
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4596
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1666
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1019
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29250
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2607
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7703
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.626280696048138e-5
allele num: 61490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11246
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

QD
type: SiteQuality
SIO_000300: 7.98e0

DP
type: SiteQuality
SIO_000300: 1.458985e6

VQSLOD
type: SiteQuality
SIO_000300: -2.7e-1

FS
type: SiteQuality
SIO_000300: 2.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450644
ensembl transcript: ENST00000554966
gene symbol: NFATC4
hgvsc: ENST00000554966.1:c.819G>A
hgvsp: ENST00000554966.1:c.819G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.779G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+508G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.744G>A
hgvsp: ENST00000555453.1:c.744G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.570G>A
hgvsp: ENST00000554661.1:c.570G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3082
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8035
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18277
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 287
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3178
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4002
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19400
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 861
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2435
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 811
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2626
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4637
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1539
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7784
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30012
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2942
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1565
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11244
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

FS
type: SiteQuality
SIO_000300: 3.334e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-1

QD
type: SiteQuality
SIO_000300: 8.33e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.54e-1

DP
type: SiteQuality
SIO_000300: 1.461981e6

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.571C>A
hgvsp: ENST00000554661.1:c.571C>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+509C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1074C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.877C>A
hgvsp: ENST00000539237.2:c.877C>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+509C>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 2440
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 853
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2963
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3917
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8066
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3164
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 813
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18364
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19503
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 981
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7834
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1539
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 615
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4538
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2633
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.737730459620878e-5
allele num: 61616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5934
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.543e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

QD
type: SiteQuality
SIO_000300: 1.099e1

VQSLOD
type: SiteQuality
SIO_000300: 7.18e-1

DP
type: SiteQuality
SIO_000300: 1.464891e6

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.42e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+509C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451454
ensembl transcript: ENST00000556169
gene symbol: NFATC4
hgvsc: ENST00000556169.1:c.745C>T
hgvsp: ENSP00000451454.1:p.Arg249Trp
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1074C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.902C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000396788
ensembl transcript: ENST00000422617
gene symbol: NFATC4
hgvsc: ENST00000422617.3:c.745C>T
hgvsp: ENSP00000396788.3:p.Arg249Trp
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 3164
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 813
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2963
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18364
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 853
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2440
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3917
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8066
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19503
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2633
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7834
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1539
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4538
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 355
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2967
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.62295507660348e-5
allele num: 61616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.42e-1

DP
type: SiteQuality
SIO_000300: 1.464891e6

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

FS
type: SiteQuality
SIO_000300: 1.543e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.099e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.982G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.878G>A
hgvsp: ENSP00000451502.1:p.Arg293Gln
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.781G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.782G>A
hgvsp: ENSP00000450590.1:p.Arg261Gln
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000250373
ensembl transcript: ENST00000250373
gene symbol: NFATC4
hgvsc: ENST00000250373.4:c.782G>A
hgvsp: ENSP00000250373.4:p.Arg261Gln
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 291
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 18725
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 821
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 815
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2612
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3151
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3741
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8090
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19698
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2438
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1580
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31184
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4613
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7978
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2649
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2998
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8676
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.774937877174299e-4
allele num: 11268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61764
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 3.713e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.84e-1

DP
type: SiteQuality
SIO_000300: 1.470899e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.119e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.573G>A
hgvsp: ENST00000557451.1:c.573G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000250373
ensembl transcript: ENST00000250373
gene symbol: NFATC4
hgvsc: ENST00000250373.4:c.783G>A
hgvsp: ENST00000250373.4:c.783G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451151
ensembl transcript: ENST00000554050
gene symbol: NFATC4
hgvsc: ENST00000554050.1:c.783G>A
hgvsp: ENST00000554050.1:c.783G>A(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.983G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+511G>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 18794
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19763
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 803
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 819
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3691
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 51
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 290
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2448
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3102
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2508
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 8164
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1373
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4498
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1587
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7994
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3006
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31222
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 9.75e1
variant carriers: 8

African
type: Population
allele count: 8
allele frequency: 9.252833680314596e-4
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5926
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

FS
type: SiteQuality
SIO_000300: 1.829e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 1.474422e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.37e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.904G>C
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000452270
ensembl transcript: ENST00000556279
gene symbol: NFATC4
hgvsc: ENST00000556279.1:c.879G>C
hgvsp: ENST00000556279.1:c.879G>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451224
ensembl transcript: ENST00000555590
gene symbol: NFATC4
hgvsc: ENST00000555590.1:c.822G>C
hgvsp: ENST00000555590.1:c.822G>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450644
ensembl transcript: ENST00000554966
gene symbol: NFATC4
hgvsc: ENST00000554966.1:c.822G>C
hgvsp: ENST00000554966.1:c.822G>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 2508
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 803
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2448
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18794
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8164
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3102
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3691
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19763
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 819
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 290
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4498
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1373
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31222
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 243
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7994
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1587
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3006
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.884150675195451e-5
allele num: 11256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5926
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61706
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

DP
type: SiteQuality
SIO_000300: 1.474422e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.96e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.829e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.793C>T
hgvsp: ENSP00000450590.1:p.Pro265Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.757C>T
hgvsp: ENSP00000450686.1:p.Pro253Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.993C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000396788
ensembl transcript: ENST00000422617
gene symbol: NFATC4
hgvsc: ENST00000422617.3:c.757C>T
hgvsp: ENSP00000396788.3:p.Pro253Ser
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 1557
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 646
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8384
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2852
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2486
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 293
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 827
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19959
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20434
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2976
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1123
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 603
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2788
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4217
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33296
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3180
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8299
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6028
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.605548776571832e-5
allele num: 62284
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.919e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.775e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

QD
type: SiteQuality
SIO_000300: 8.619999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.331e0

DP
type: SiteQuality
SIO_000300: 1.499808e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+523A>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1088A>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.759A>G
hgvsp: ENST00000555453.1:c.759A>G(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.995A>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+523A>G
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 829
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2962
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 19974
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8409
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20546
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 294
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2475
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2792
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 617
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1519
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8351
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33302
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4190
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2800
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.604312391708914e-5
allele num: 62332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16314
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 6.73e0

DP
type: SiteQuality
SIO_000300: 1.502129e6

VQSLOD
type: SiteQuality
SIO_000300: -5.261e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.94e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451454
ensembl transcript: ENST00000556169
gene symbol: NFATC4
hgvsc: ENST00000556169.1:c.774C>T
hgvsp: ENST00000556169.1:c.774C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.931C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.999C>T
hgvsp: ENST00000413692.2:c.999C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.600C>T
hgvsp: ENST00000557451.1:c.600C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+538C>T
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21209
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20036
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8639
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2502
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2756
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2375
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 297
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1285
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 839
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33820
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8683
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 657
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3302
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3892
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.111722283339445e-5
allele num: 16362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6122
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.004e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 2.96e1

FS
type: SiteQuality
SIO_000300: 2.626e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.51941e6

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451224
ensembl transcript: ENST00000555590
gene symbol: NFATC4
hgvsc: ENST00000555590.1:c.857G>A
hgvsp: ENSP00000451224.1:p.Ser286Asn
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+546G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1111G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.608G>A
hgvsp: ENSP00000451284.1:p.Ser203Asn
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.608G>A
hgvsp: ENSP00000450733.1:p.Ser203Asn
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 2194
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1150
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2635
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21445
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 475
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20134
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8740
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2516
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 841
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3322
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8783
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2925
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3663
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 298
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34199
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.589370291490511e-5
allele num: 62918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.307e-1

QD
type: SiteQuality
SIO_000300: 1.178e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.884e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.388e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.64e-1

DP
type: SiteQuality
SIO_000300: 1.526182e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.822G>C
hgvsp: ENST00000553708.1:c.822G>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.612G>C
hgvsp: ENST00000554661.1:c.612G>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.1022G>C
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+550G>C
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451224
ensembl transcript: ENST00000555590
gene symbol: NFATC4
hgvsc: ENST00000555590.1:c.861G>C
hgvsp: ENST00000555590.1:c.861G>C(p.%3D)
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 296
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2525
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 20014
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1143
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 845
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2530
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2122
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 495
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 21647
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8805
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8823
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2944
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1691
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3528
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34252
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62932
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.220256253813301e-4
allele num: 16390
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.664e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

FS
type: SiteQuality
SIO_000300: 1.2842e1

QD
type: SiteQuality
SIO_000300: 1.076e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.932e0

DP
type: SiteQuality
SIO_000300: 1.530159e6

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.924C>G
hgvsp: ENST00000553469.1:c.924C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.949C>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.828C>G
hgvsp: ENST00000553708.1:c.828C>G(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+556C>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1121C>G
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 842
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1203
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8842
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2524
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2072
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21822
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 298
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 19901
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 516
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 124
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3365
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1701
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3445
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34378
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.829491401390413e-4
allele num: 16398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.169773044250032e-5
allele num: 63096
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.115e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 1.107e0

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

DP
type: SiteQuality
SIO_000300: 1.532927e6

QD
type: SiteQuality
SIO_000300: 1.137e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+566G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.838G>A
hgvsp: ENSP00000450590.1:p.Ala280Thr
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388668
ensembl transcript: ENST00000424781
gene symbol: NFATC4
hgvsc: ENST00000424781.2:c.877G>A
hgvsp: ENSP00000388668.2:p.Ala293Thr
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.628G>A
hgvsp: ENSP00000451284.1:p.Ala210Thr
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+566G>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 591
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2293
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2004
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19456
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 847
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22089
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8933
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2543
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1362
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 297
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8965
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3384
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3144
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2970
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33802
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584283903675539e-5
allele num: 63120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.807e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.631e0

VQSLOD
type: SiteQuality
SIO_000300: 6.879999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.878e0

DP
type: SiteQuality
SIO_000300: 1.535215e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.547e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.934G>C
hgvsp: ENSP00000451502.1:p.Ala312Pro
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450644
ensembl transcript: ENST00000554966
gene symbol: NFATC4
hgvsc: ENST00000554966.1:c.877G>C
hgvsp: ENSP00000450644.1:p.Ala293Pro
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.628G>C
hgvsp: ENSP00000451284.1:p.Ala210Pro
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.837G>C
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 2543
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 847
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8933
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2004
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22089
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 591
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1362
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 297
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2293
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19456
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3144
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8965
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33802
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3384
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584283903675539e-5
allele num: 63120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8954
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.535215e6

FS
type: SiteQuality
SIO_000300: 3.878e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.547e0

VQSLOD
type: SiteQuality
SIO_000300: 6.879999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.631e0

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

QD
type: SiteQuality
SIO_000300: 1.807e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.935C>T
hgvsp: ENSP00000451502.1:p.Ala312Val
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000452039
ensembl transcript: ENST00000554591
gene symbol: NFATC4
hgvsc: ENST00000554591.1:c.1028C>T
hgvsp: ENSP00000452039.1:p.Ala343Val
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1132C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000250373
ensembl transcript: ENST00000250373
gene symbol: NFATC4
hgvsc: ENST00000250373.4:c.839C>T
hgvsp: ENSP00000250373.4:p.Ala280Val
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 1993
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2552
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 588
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22130
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1333
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19416
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2278
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 299
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8973
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 852
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 614
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2969
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3386
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1705
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8978
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.166962249809982e-5
allele num: 63152
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.103515625e-5
allele num: 16384
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.178967224711153e-4
allele num: 8482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8962
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.376e0

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

QD
type: SiteQuality
SIO_000300: 1.041e1

DP
type: SiteQuality
SIO_000300: 1.536747e6

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.632C>T
hgvsp: ENSP00000451284.1:p.Ser211Phe
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.938C>T
hgvsp: ENSP00000439350.2:p.Ser313Phe
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+570C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.806C>T
hgvsp: ENSP00000450686.1:p.Ser269Phe
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1970
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1281
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22278
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 612
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2229
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9011
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19331
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 850
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 298
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2555
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2966
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8996
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1715
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3406
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34237
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.582779360557138e-5
allele num: 63180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 1.538622e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.755e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

QD
type: SiteQuality
SIO_000300: 1.304e1

VQSLOD
type: SiteQuality
SIO_000300: 8.44e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450590
ensembl transcript: ENST00000553708
gene symbol: NFATC4
hgvsc: ENST00000553708.1:c.844C>T
hgvsp: ENSP00000450590.1:p.Pro282Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1137C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.1044C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.634C>T
hgvsp: ENSP00000451284.1:p.Pro212Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.940C>T
hgvsp: ENSP00000451502.1:p.Pro314Ser
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 297
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22242
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1360
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19244
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2193
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 659
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1959
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9043
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2559
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 850
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8964
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 708
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2940
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33671
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584384308257811e-5
allele num: 63116
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.537783e6

MQRankSum
type: SiteQuality
SIO_000300: -1.12e0

FS
type: SiteQuality
SIO_000300: 8.613e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e-1

QD
type: SiteQuality
SIO_000300: 1.441e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+581T>C
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.643T>C
hgvsp: ENSP00000451284.1:p.Ser215Pro
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.643T>C
hgvsp: ENSP00000450733.1:p.Ser215Pro
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1146T>C
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.974T>C
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9091
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22502
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2106
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1466
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 717
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1907
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 855
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2556
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18881
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 302
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 658
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1708
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8866
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3411
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.128668171557562e-4
allele num: 8860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63022
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

FS
type: SiteQuality
SIO_000300: 4.129e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

VQSLOD
type: SiteQuality
SIO_000300: -2.185e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 5.816e1

DP
type: SiteQuality
SIO_000300: 1.539385e6

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.955C>A
hgvsp: ENSP00000439350.2:p.Arg319Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.649C>A
hgvsp: ENSP00000451284.1:p.Arg217Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.1059C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.858C>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.1048C>A
hgvsp: ENSP00000388910.2:p.Arg350Ser
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 1340
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1778
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22864
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2075
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 865
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 299
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 733
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2551
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18719
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9171
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3016
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1726
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33835
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 199
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3433
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8937
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584484725567246e-5
allele num: 63112
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.0e1

DP
type: SiteQuality
SIO_000300: 1.544537e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.18e-1

FS
type: SiteQuality
SIO_000300: 7.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451224
ensembl transcript: ENST00000555590
gene symbol: NFATC4
hgvsc: ENST00000555590.1:c.898C>T
hgvsp: ENSP00000451224.1:p.Arg300Cys
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.955C>T
hgvsp: ENSP00000451502.1:p.Arg319Cys
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+587C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.649C>T
hgvsp: ENSP00000451284.1:p.Arg217Cys
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 2551
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 733
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18719
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1340
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 22864
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 865
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2075
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 299
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9171
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1778
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3016
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3433
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8937
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1726
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 521
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33835
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8906
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.113216774666829e-5
allele num: 16358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.173708920187793e-4
allele num: 8520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63112
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.78e-1

DP
type: SiteQuality
SIO_000300: 1.544537e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000396788
ensembl transcript: ENST00000422617
gene symbol: NFATC4
hgvsc: ENST00000422617.3:c.834G>T
hgvsp: ENST00000422617.3:c.834G>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+598G>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.991G>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.869G>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1163G>T
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 9239
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 697
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 298
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1670
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18773
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2042
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 862
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23029
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1231
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2579
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9025
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33845
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2679
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3471
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.119951040391677e-5
allele num: 16340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8910
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.013e0

FS
type: SiteQuality
SIO_000300: 1.441e0

QD
type: SiteQuality
SIO_000300: 9.699999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -6.587e-1

DP
type: SiteQuality
SIO_000300: 1.549581e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.83e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: -1.198e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.979T>A
hgvsp: ENSP00000439350.2:p.Ser327Thr
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.847T>A
hgvsp: ENSP00000450686.1:p.Ser283Thr
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.673T>A
hgvsp: ENSP00000450733.1:p.Ser225Thr
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000452349
ensembl transcript: ENST00000553879
gene symbol: NFATC4
hgvsc: ENST00000553879.1:c.673T>A
hgvsp: ENSP00000452349.1:p.Ser225Thr
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 2053
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 847
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23081
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2572
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 548
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1209
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19105
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9192
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1537
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3081
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3480
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9115
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34556
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8938
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.576342255430499e-5
allele num: 63438
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.451e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.825e1

QD
type: SiteQuality
SIO_000300: 1.399e1

FS
type: SiteQuality
SIO_000300: 6.978e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

DP
type: SiteQuality
SIO_000300: 1.553423e6

VQSLOD
type: SiteQuality
SIO_000300: -1.793e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.254e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556302
gene symbol: NFATC4
hgvsc: ENST00000556302.1:n.892C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+621C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450644
ensembl transcript: ENST00000554966
gene symbol: NFATC4
hgvsc: ENST00000554966.1:c.932C>T
hgvsp: ENSP00000450644.1:p.Pro311Leu
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1186C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.683C>T
hgvsp: ENSP00000450733.1:p.Pro228Leu
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 19370
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23166
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1943
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1100
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 290
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 839
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 536
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2544
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1450
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9197
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3083
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2607
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 664
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3492
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9158
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34916
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.570746418698165e-5
allele num: 63664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8994
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

QD
type: SiteQuality
SIO_000300: 2.688e1

MQRankSum
type: SiteQuality
SIO_000300: -8.81e-1

DP
type: SiteQuality
SIO_000300: 1.556489e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.407e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.821e0

VQSLOD
type: SiteQuality
SIO_000300: -2.374e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+623C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.991C>T
hgvsp: ENSP00000439350.2:p.Pro331Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451224
ensembl transcript: ENST00000555590
gene symbol: NFATC4
hgvsc: ENST00000555590.1:c.934C>T
hgvsp: ENSP00000451224.1:p.Pro312Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.1084C>T
hgvsp: ENSP00000388910.2:p.Pro362Ser
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.1095C>T
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 1919
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23191
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1092
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1440
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2551
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 836
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9186
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 292
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 551
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 19371
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 104
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 6
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34794
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3488
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9147
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 3084
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2513
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.182380216383308e-4
allele num: 6470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.099453414588176e-4
allele num: 63668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8986
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.152073732718894e-3
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e-1

QD
type: SiteQuality
SIO_000300: 1.26e1

FS
type: SiteQuality
SIO_000300: 5.459e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.264e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

DP
type: SiteQuality
SIO_000300: 1.556885e6

MQ
type: SiteQuality
SIO_000300: 5.937e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451284
ensembl transcript: ENST00000557451
gene symbol: NFATC4
hgvsc: ENST00000557451.1:c.693C>T
hgvsp: ENST00000557451.1:c.693C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.867C>T
hgvsp: ENST00000555453.1:c.867C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.693C>T
hgvsp: ENST00000554661.1:c.693C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.1092C>T
hgvsp: ENST00000413692.2:c.1092C>T(p.%3D)
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2540
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 943
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23410
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19565
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1811
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 564
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9144
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 291
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 839
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1320
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35339
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3089
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 274
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3502
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1754
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9166
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8988
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.567054251418184e-5
allele num: 63814
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.95e-1

FS
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

QD
type: SiteQuality
SIO_000300: 1.472e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.560685e6

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000388910
ensembl transcript: ENST00000413692
gene symbol: NFATC4
hgvsc: ENST00000413692.2:c.1093C>G
hgvsp: ENSP00000388910.2:p.Pro365Ala
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+632C>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+632C>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1197C>G
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.868C>G
hgvsp: ENSP00000450686.1:p.Pro290Ala
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 560
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2540
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9143
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 23422
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 912
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19620
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 840
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1290
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 292
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1809
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3090
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1752
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3504
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 621
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35542
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9170
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.566121656330264e-5
allele num: 63852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

DP
type: SiteQuality
SIO_000300: 1.561303e6

QD
type: SiteQuality
SIO_000300: 1.233e1

FS
type: SiteQuality
SIO_000300: 4.229e0

MQRankSum
type: SiteQuality
SIO_000300: -6.72e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.1007C>T
hgvsp: ENSP00000439350.2:p.Pro336Leu
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000440487
gene symbol: NFATC4
hgvsc: ENST00000440487.2:n.1111C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451992
ensembl transcript: ENST00000554779
gene symbol: NFATC4
hgvsc: ENST00000554779.1:c.272+639C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000557028
gene symbol: NFATC4
hgvsc: ENST00000557028.1:n.427+639C>T
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.1032C>T
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 1726
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 291
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 879
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 835
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19639
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 602
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9146
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1234
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23522
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2535
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35475
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3481
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1751
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3079
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 9.75e1
variant carriers: 3

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8994
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.700131603684903e-5
allele num: 63828
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.654e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.17e-1

DP
type: SiteQuality
SIO_000300: 1.562548e6

MQRankSum
type: SiteQuality
SIO_000300: 2.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.329e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 6.669e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000452039
ensembl transcript: ENST00000554591
gene symbol: NFATC4
hgvsc: ENST00000554591.1:c.1106C>T
hgvsp: ENSP00000452039.1:p.Ala369Val
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000451502
ensembl transcript: ENST00000553469
gene symbol: NFATC4
hgvsc: ENST00000553469.1:c.1013C>T
hgvsp: ENSP00000451502.1:p.Ala338Val
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.881C>T
hgvsp: ENSP00000450686.1:p.Ala294Val
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.1013C>T
hgvsp: ENSP00000439350.2:p.Ala338Val
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 843
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1635
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1186
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9206
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 647
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2541
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 841
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23648
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19547
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3072
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35217
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1750
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3474
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9129
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16316
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.569168968114487e-5
allele num: 63728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

FS
type: SiteQuality
SIO_000300: 4.737e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e-1

DP
type: SiteQuality
SIO_000300: 1.564647e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.56e-1

QD
type: SiteQuality
SIO_000300: 1.18e1

VQSLOD
type: SiteQuality
SIO_000300: -7.658e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.257e0

MQRankSum
type: SiteQuality
SIO_000300: -1.749e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450733
ensembl transcript: ENST00000554661
gene symbol: NFATC4
hgvsc: ENST00000554661.1:c.710G>A
hgvsp: ENSP00000450733.1:p.Arg237Gln
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000450686
ensembl transcript: ENST00000555453
gene symbol: NFATC4
hgvsc: ENST00000555453.1:c.884G>A
hgvsp: ENSP00000450686.1:p.Arg295Gln
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000556957
gene symbol: NFATC4
hgvsc: ENST00000556957.1:n.1041G>A
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000100968
ensembl protein: ENSP00000439350
ensembl transcript: ENST00000539237
gene symbol: NFATC4
hgvsc: ENST00000539237.2:c.1016G>A
hgvsp: ENSP00000439350.2:p.Arg339Gln
variant of: http://identifiers.org/hgnc/7778

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000100968
ensembl transcript: ENST00000554655
gene symbol: NFATC4
hgvsc: ENST00000554655.1:n.1213G>A
variant of: http://identifiers.org/hgnc/7778

GenotypeDepth
all individuals: 23774
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 7.25e1
variant carriers: 0