16-68225167-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225167
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225165
    reference: chr 16
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2923_2924delTT
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2596_2597delTT
  hgvsp: ENSP00000264008.6:p.Leu866SerfsTer34
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2641_2642delTT
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2596_2597delTT
  hgvsp: ENSP00000331324.4:p.Leu866SerfsTer34
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2554_2555delTT
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2641_2642delTT
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2549_2550delTT
  hgvsp: ENSP00000456379.1:p.Leu851SerfsTer34
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1181_*1182delTT
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2596_2597delTT
  hgvsp: ENSP00000460533.1:p.Leu866SerfsTer34
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2620_2621delTT
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2923_2924delTT
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2549_2550delTT
  hgvsp: ENSP00000456120.1:p.Leu851SerfsTer34
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2591_2592delTT
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2554_2555delTT
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.2995_2996delTT
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2923_2924delTT
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2596_2597delTT
  hgvsp: ENSP00000300659.5:p.Leu866SerfsTer34
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu866SerfsTer34
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: CTT
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

16-68225176-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225176
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225176
    reference: chr 16
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3003T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2931T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1189T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2604T>C
  hgvsp: ENST00000349223.5:c.2604T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2557T>C
  hgvsp: ENST00000570212.1:c.2557T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2931T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2604T>C
  hgvsp: ENST00000329524.4:c.2604T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2562T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2649T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2604T>C
  hgvsp: ENST00000575270.1:c.2604T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2604T>C
  hgvsp: ENST00000346183.3:c.2604T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2562T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2599T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2557T>C
  hgvsp: ENST00000562926.1:c.2557T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2628T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2649T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2931T>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His868His
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-68225180-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225180
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225180
    reference: chr 16
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2935C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2608C>T
  hgvsp: ENSP00000460533.1:p.Pro870Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2608C>T
  hgvsp: ENSP00000331324.4:p.Pro870Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2653C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2632C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2603C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2608C>T
  hgvsp: ENSP00000300659.5:p.Pro870Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2608C>T
  hgvsp: ENSP00000264008.6:p.Pro870Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2935C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2653C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2935C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2566C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1193C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2561C>T
  hgvsp: ENSP00000456120.1:p.Pro855Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2561C>T
  hgvsp: ENSP00000456379.1:p.Pro855Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3007C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2566C>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro870Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

16-68225197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225197
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225197
    reference: chr 16
allele count: 8
allele frequency: 6.589243060703402e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2649C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2583C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2625C>T
  hgvsp: ENST00000346183.3:c.2625C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2578C>T
  hgvsp: ENST00000570212.1:c.2578C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2670C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2583C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2625C>T
  hgvsp: ENST00000329524.4:c.2625C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2952C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2625C>T
  hgvsp: ENST00000575270.1:c.2625C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2625C>T
  hgvsp: ENST00000349223.5:c.2625C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1210C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2620C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2952C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2670C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2578C>T
  hgvsp: ENST00000562926.1:c.2578C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2952C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3024C>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr875Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

16-68225198-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225198
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225198
    reference: chr 16
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2584C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2626C>G
  hgvsp: ENSP00000300659.5:p.Leu876Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2579C>G
  hgvsp: ENSP00000456120.1:p.Leu861Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2953C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2626C>G
  hgvsp: ENSP00000460533.1:p.Leu876Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2621C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2953C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1211C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2650C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2626C>G
  hgvsp: ENSP00000331324.4:p.Leu876Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2579C>G
  hgvsp: ENSP00000456379.1:p.Leu861Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2671C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2584C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2953C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2626C>G
  hgvsp: ENSP00000264008.6:p.Leu876Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3025C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2671C>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu876Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

16-68225205-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225205
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225205
    reference: chr 16
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2960A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2633A>T
  hgvsp: ENSP00000264008.6:p.His878Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2960A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2628A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3032A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2633A>T
  hgvsp: ENSP00000331324.4:p.His878Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2633A>T
  hgvsp: ENSP00000300659.5:p.His878Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2591A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1218A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2678A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2633A>T
  hgvsp: ENSP00000460533.1:p.His878Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2586A>T
  hgvsp: ENSP00000456120.1:p.His863Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2586A>T
  hgvsp: ENSP00000456379.1:p.His863Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2657A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2960A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2678A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2591A>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His878Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

16-68225208-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225208
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225208
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1221T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2636T>C
  hgvsp: ENSP00000264008.6:p.Leu879Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2589T>C
  hgvsp: ENSP00000456120.1:p.Leu864Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2681T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2636T>C
  hgvsp: ENSP00000331324.4:p.Leu879Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2636T>C
  hgvsp: ENSP00000460533.1:p.Leu879Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2594T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2681T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2660T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2963T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2963T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2594T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3035T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2636T>C
  hgvsp: ENSP00000300659.5:p.Leu879Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2589T>C
  hgvsp: ENSP00000456379.1:p.Leu864Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2631T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2963T>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10149
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu879Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/16-68225211-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225211
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225211
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2597A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2639A>C
  hgvsp: ENSP00000300659.5:p.Gln880Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2592A>C
  hgvsp: ENSP00000456379.1:p.Gln865Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2597A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2639A>C
  hgvsp: ENSP00000460533.1:p.Gln880Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1224A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2634A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2966A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2592A>C
  hgvsp: ENSP00000456120.1:p.Gln865Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3038A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2966A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2639A>C
  hgvsp: ENSP00000331324.4:p.Gln880Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2639A>C
  hgvsp: ENSP00000264008.6:p.Gln880Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2684A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2663A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2684A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2966A>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln880Pro
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

16-68225212-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225212
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225212
    reference: chr 16
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2593A>G
  hgvsp: ENST00000570212.1:c.2593A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2598A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2640A>G
  hgvsp: ENST00000346183.3:c.2640A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2640A>G
  hgvsp: ENST00000329524.4:c.2640A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2640A>G
  hgvsp: ENST00000575270.1:c.2640A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2635A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2685A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2598A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2640A>G
  hgvsp: ENST00000349223.5:c.2640A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2967A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2967A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2967A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3039A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2593A>G
  hgvsp: ENST00000562926.1:c.2593A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2664A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1225A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2685A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln880Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

16-68225215-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225215
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225215
    reference: chr 16
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2596A>G
  hgvsp: ENST00000562926.1:c.2596A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2601A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2643A>G
  hgvsp: ENST00000346183.3:c.2643A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2638A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2596A>G
  hgvsp: ENST00000570212.1:c.2596A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2970A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2643A>G
  hgvsp: ENST00000329524.4:c.2643A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2643A>G
  hgvsp: ENST00000349223.5:c.2643A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1228A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2970A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2970A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3042A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2643A>G
  hgvsp: ENST00000575270.1:c.2643A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2667A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2688A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2601A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2688A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5434
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser881Ser
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

16-68225216-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225216
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225216
    reference: chr 16
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2689A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1229A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2971A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2644A>G
  hgvsp: ENSP00000460533.1:p.Met882Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2668A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2597A>G
  hgvsp: ENSP00000456379.1:p.Met867Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2644A>G
  hgvsp: ENSP00000331324.4:p.Met882Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2602A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2602A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2644A>G
  hgvsp: ENSP00000264008.6:p.Met882Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2597A>G
  hgvsp: ENSP00000456120.1:p.Met867Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2971A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3043A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2689A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2644A>G
  hgvsp: ENSP00000300659.5:p.Met882Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2971A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2639A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met882Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-68225219-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225219
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225219
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3046G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2974G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2647G>A
  hgvsp: ENSP00000264008.6:p.Gly883Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2605G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2692G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2642G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2974G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2647G>A
  hgvsp: ENSP00000331324.4:p.Gly883Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2600G>A
  hgvsp: ENSP00000456379.1:p.Gly868Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2671G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2647G>A
  hgvsp: ENSP00000460533.1:p.Gly883Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1232G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2647G>A
  hgvsp: ENSP00000300659.5:p.Gly883Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2600G>A
  hgvsp: ENSP00000456120.1:p.Gly868Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2692G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2974G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2605G>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly883Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

16-68225239-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225239
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225239
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2667A>G
  hgvsp: ENST00000349223.5:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.2994A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.2994A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2691A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2667A>G
  hgvsp: ENST00000329524.4:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2662A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.2994A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1252A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2620A>G
  hgvsp: ENST00000570212.1:c.2620A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2667A>G
  hgvsp: ENST00000575270.1:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2712A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2620A>G
  hgvsp: ENST00000562926.1:c.2620A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2667A>G
  hgvsp: ENST00000346183.3:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2625A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3066A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2625A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2712A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr889Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

16-68225247-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225247
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225247
    reference: chr 16
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2633G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2699G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2670G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2633G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2628G>T
  hgvsp: ENSP00000456379.1:p.Arg877Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2675G>T
  hgvsp: ENSP00000331324.4:p.Arg892Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2675G>T
  hgvsp: ENSP00000460533.1:p.Arg892Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2628G>T
  hgvsp: ENSP00000456120.1:p.Arg877Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2675G>T
  hgvsp: ENSP00000300659.5:p.Arg892Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2675G>T
  hgvsp: ENSP00000264008.6:p.Arg892Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3002G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1260G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2720G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2720G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3074G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3002G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3002G>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg892Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

16-68225251-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225251
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225251
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2724T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2637T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2679T>A
  hgvsp: ENST00000575270.1:c.2679T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1264T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2703T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2724T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3006T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2632T>A
  hgvsp: ENST00000562926.1:c.2632T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3078T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2679T>A
  hgvsp: ENST00000349223.5:c.2679T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2632T>A
  hgvsp: ENST00000570212.1:c.2632T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3006T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2679T>A
  hgvsp: ENST00000346183.3:c.2679T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2679T>A
  hgvsp: ENST00000329524.4:c.2679T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2674T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2637T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3006T>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser893Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

16-68225258-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225258
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225258
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2639T>A
  hgvsp: ENSP00000456120.1:p.Ser881Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3085T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3013T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2686T>A
  hgvsp: ENSP00000460533.1:p.Ser896Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2710T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2731T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2686T>A
  hgvsp: ENSP00000264008.6:p.Ser896Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2639T>A
  hgvsp: ENSP00000456379.1:p.Ser881Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2686T>A
  hgvsp: ENSP00000300659.5:p.Ser896Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2686T>A
  hgvsp: ENSP00000331324.4:p.Ser896Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2731T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3013T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2681T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2644T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2644T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3013T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1271T>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser896Thr
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

16-68225259-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225259
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225259
    reference: chr 16
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2687C>T
  hgvsp: ENSP00000331324.4:p.Ser896Phe
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2640C>T
  hgvsp: ENSP00000456120.1:p.Ser881Phe
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3014C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2687C>T
  hgvsp: ENSP00000460533.1:p.Ser896Phe
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2732C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2640C>T
  hgvsp: ENSP00000456379.1:p.Ser881Phe
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2682C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2711C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2687C>T
  hgvsp: ENSP00000300659.5:p.Ser896Phe
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1272C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2687C>T
  hgvsp: ENSP00000264008.6:p.Ser896Phe
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2645C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3086C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2732C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2645C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3014C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3014C>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser896Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

16-68225265-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225265
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225265
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3092T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2717T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2693T>C
  hgvsp: ENSP00000331324.4:p.Val898Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2688T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3020T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2651T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2693T>C
  hgvsp: ENSP00000264008.6:p.Val898Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2693T>C
  hgvsp: ENSP00000460533.1:p.Val898Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3020T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2646T>C
  hgvsp: ENSP00000456120.1:p.Val883Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2646T>C
  hgvsp: ENSP00000456379.1:p.Val883Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3020T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2738T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2651T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2693T>C
  hgvsp: ENSP00000300659.5:p.Val898Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1278T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2738T>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val898Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

16-68225270-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225270
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225270
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2743G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2698G>A
  hgvsp: ENSP00000300659.5:p.Asp900Asn
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1283G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2656G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3025G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2743G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3025G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2651G>A
  hgvsp: ENSP00000456120.1:p.Asp885Asn
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2693G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2722G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2698G>A
  hgvsp: ENSP00000264008.6:p.Asp900Asn
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2698G>A
  hgvsp: ENSP00000460533.1:p.Asp900Asn
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2698G>A
  hgvsp: ENSP00000331324.4:p.Asp900Asn
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2651G>A
  hgvsp: ENSP00000456379.1:p.Asp885Asn
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3097G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3025G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2656G>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp900Asn
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

16-68225276-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225276
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225276
    reference: chr 16
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3031A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2662A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2657A>G
  hgvsp: ENSP00000456120.1:p.Ile887Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2657A>G
  hgvsp: ENSP00000456379.1:p.Ile887Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2749A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3031A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2728A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2749A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3103A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2704A>G
  hgvsp: ENSP00000264008.6:p.Ile902Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2662A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2699A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2704A>G
  hgvsp: ENSP00000331324.4:p.Ile902Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2704A>G
  hgvsp: ENSP00000460533.1:p.Ile902Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2704A>G
  hgvsp: ENSP00000300659.5:p.Ile902Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1289A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3031A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile902Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

16-68225282-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225282
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225282
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2755G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2668G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3109G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2710G>C
  hgvsp: ENSP00000460533.1:p.Gly904Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1295G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2755G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2710G>C
  hgvsp: ENSP00000264008.6:p.Gly904Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2668G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2663G>C
  hgvsp: ENSP00000456379.1:p.Gly889Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2663G>C
  hgvsp: ENSP00000456120.1:p.Gly889Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3037G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2734G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2710G>C
  hgvsp: ENSP00000300659.5:p.Gly904Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2710G>C
  hgvsp: ENSP00000331324.4:p.Gly904Arg
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3037G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3037G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2705G>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly904Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

16-68225288-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225288
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225288
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2716C>G
  hgvsp: ENSP00000331324.4:p.Pro906Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2711C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3043C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2716C>G
  hgvsp: ENSP00000300659.5:p.Pro906Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2674C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3115C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2716C>G
  hgvsp: ENSP00000264008.6:p.Pro906Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2669C>G
  hgvsp: ENSP00000456120.1:p.Pro891Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3043C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2669C>G
  hgvsp: ENSP00000456379.1:p.Pro891Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2740C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1301C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2761C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2674C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2716C>G
  hgvsp: ENSP00000460533.1:p.Pro906Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2761C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3043C>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro906Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

16-68225290-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225290
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225290
    reference: chr 16
allele count: 5
allele frequency: 4.118276912939626e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2718T>C
  hgvsp: ENST00000346183.3:c.2718T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3117T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2671T>C
  hgvsp: ENST00000570212.1:c.2671T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2763T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3045T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2718T>C
  hgvsp: ENST00000575270.1:c.2718T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2718T>C
  hgvsp: ENST00000349223.5:c.2718T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2718T>C
  hgvsp: ENST00000329524.4:c.2718T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1303T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2676T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2763T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2713T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2676T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2671T>C
  hgvsp: ENST00000562926.1:c.2671T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3045T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2742T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3045T>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12261
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro906Pro
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

16-68225291-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225291
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225291
    reference: chr 16
allele count: 17
allele frequency: 1.400191084900998e-4
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2719T>C
  hgvsp: ENSP00000264008.6:p.Ser907Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2719T>C
  hgvsp: ENSP00000460533.1:p.Ser907Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2677T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2677T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2764T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3046T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3046T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2672T>C
  hgvsp: ENSP00000456120.1:p.Ser892Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2719T>C
  hgvsp: ENSP00000331324.4:p.Ser907Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3046T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2719T>C
  hgvsp: ENSP00000300659.5:p.Ser907Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2672T>C
  hgvsp: ENSP00000456379.1:p.Ser892Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2743T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3118T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2764T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1304T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2714T>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser907Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

16-68225292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225292
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225292
    reference: chr 16
allele count: 11
allele frequency: 9.060059961124106e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2720C>T
  hgvsp: ENSP00000300659.5:p.Ser907Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2765C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3047C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2673C>T
  hgvsp: ENSP00000456120.1:p.Ser892Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2715C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2720C>T
  hgvsp: ENSP00000460533.1:p.Ser907Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2678C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2720C>T
  hgvsp: ENSP00000264008.6:p.Ser907Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2720C>T
  hgvsp: ENSP00000331324.4:p.Ser907Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2673C>T
  hgvsp: ENSP00000456379.1:p.Ser892Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3119C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3047C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2765C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3047C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2678C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1305C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2744C>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser907Leu
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ

16-68225293-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225293
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225293
    reference: chr 16
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2721G>A
  hgvsp: ENST00000346183.3:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2679G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3120G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2674G>A
  hgvsp: ENST00000562926.1:c.2674G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2766G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3048G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2721G>A
  hgvsp: ENST00000575270.1:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2716G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2721G>A
  hgvsp: ENST00000329524.4:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2721G>A
  hgvsp: ENST00000349223.5:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1306G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2674G>A
  hgvsp: ENST00000570212.1:c.2674G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3048G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2745G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2766G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2679G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3048G>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser907Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

http://identifiers.org/exac.variant/16-68225298-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225298
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225298
    reference: chr 16
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3125A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2771A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2679A>C
  hgvsp: ENSP00000456379.1:p.Gln894Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2771A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2726A>C
  hgvsp: ENSP00000460533.1:p.Gln909Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1311A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2726A>C
  hgvsp: ENSP00000300659.5:p.Gln909Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2750A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3053A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2679A>C
  hgvsp: ENSP00000456120.1:p.Gln894Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2726A>C
  hgvsp: ENSP00000331324.4:p.Gln909Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2726A>C
  hgvsp: ENSP00000264008.6:p.Gln909Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2684A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2721A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3053A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2684A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3053A>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln909Pro
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

16-68225299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225299
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225299
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3054G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2685G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2727G>A
  hgvsp: ENST00000575270.1:c.2727G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2727G>A
  hgvsp: ENST00000349223.5:c.2727G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3054G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2727G>A
  hgvsp: ENST00000346183.3:c.2727G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2727G>A
  hgvsp: ENST00000329524.4:c.2727G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2722G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2680G>A
  hgvsp: ENST00000570212.1:c.2680G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3126G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2751G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3054G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2772G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2685G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2680G>A
  hgvsp: ENST00000562926.1:c.2680G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1312G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2772G>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10159
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln909Gln
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-68225305-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225305
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225305
    reference: chr 16
allele count: 49
allele frequency: 4.035911374680834e-4
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2778A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3132A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2733A>C
  hgvsp: ENSP00000460533.1:p.Gln911His
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2733A>C
  hgvsp: ENSP00000300659.5:p.Gln911His
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2757A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2778A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1318A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2733A>C
  hgvsp: ENSP00000331324.4:p.Gln911His
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3060A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2686A>C
  hgvsp: ENSP00000456379.1:p.Gln896His
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3060A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2686A>C
  hgvsp: ENSP00000456120.1:p.Gln896His
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2728A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3060A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2733A>C
  hgvsp: ENSP00000264008.6:p.Gln911His
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2691A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2691A>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
hgvs: p.Gln911His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

16-68225305-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225305
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225305
    reference: chr 16
allele count: 10
allele frequency: 8.236553825879252e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2757A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2733A>G
  hgvsp: ENST00000329524.4:c.2733A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2686A>G
  hgvsp: ENST00000562926.1:c.2686A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3060A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2733A>G
  hgvsp: ENST00000349223.5:c.2733A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2691A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2728A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3060A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3132A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1318A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2733A>G
  hgvsp: ENST00000575270.1:c.2733A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2686A>G
  hgvsp: ENST00000570212.1:c.2686A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2778A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2733A>G
  hgvsp: ENST00000346183.3:c.2733A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2691A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3060A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2778A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln911Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-68225310-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225310
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225310
    reference: chr 16
allele count: 3
allele frequency: 2.470966147763776e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2696T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3065T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2691T>C
  hgvsp: ENSP00000456120.1:p.Ile898Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3137T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2738T>C
  hgvsp: ENSP00000264008.6:p.Ile913Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3065T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2738T>C
  hgvsp: ENSP00000300659.5:p.Ile913Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1323T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2733T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2738T>C
  hgvsp: ENSP00000331324.4:p.Ile913Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2738T>C
  hgvsp: ENSP00000460533.1:p.Ile913Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2691T>C
  hgvsp: ENSP00000456379.1:p.Ile898Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2696T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2762T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2783T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3065T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2783T>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile913Thr
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

16-68225312-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225312
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225312
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2693A>G
  hgvsp: ENSP00000456120.1:p.Thr899Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2698A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2735A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2740A>G
  hgvsp: ENSP00000300659.5:p.Thr914Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3067A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2740A>G
  hgvsp: ENSP00000460533.1:p.Thr914Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2740A>G
  hgvsp: ENSP00000331324.4:p.Thr914Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2693A>G
  hgvsp: ENSP00000456379.1:p.Thr899Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2740A>G
  hgvsp: ENSP00000264008.6:p.Thr914Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1325A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2785A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3139A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2785A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2698A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3067A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3067A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2764A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr914Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

16-68225314-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225314
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225314
    reference: chr 16
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2787A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2742A>G
  hgvsp: ENST00000329524.4:c.2742A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2700A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2695A>G
  hgvsp: ENST00000570212.1:c.2695A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2742A>G
  hgvsp: ENST00000575270.1:c.2742A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2695A>G
  hgvsp: ENST00000562926.1:c.2695A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2737A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2766A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1327A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3069A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3141A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2787A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2742A>G
  hgvsp: ENST00000346183.3:c.2742A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2742A>G
  hgvsp: ENST00000349223.5:c.2742A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2700A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3069A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3069A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15631
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr914Thr
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ

16-68225316-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225316
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225316
    reference: chr 16
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2744A>G
  hgvsp: ENSP00000264008.6:p.Tyr915Cys
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2744A>G
  hgvsp: ENSP00000300659.5:p.Tyr915Cys
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2744A>G
  hgvsp: ENSP00000460533.1:p.Tyr915Cys
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2702A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2697A>G
  hgvsp: ENSP00000456379.1:p.Tyr900Cys
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2739A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2702A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3071A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2697A>G
  hgvsp: ENSP00000456120.1:p.Tyr900Cys
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2768A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2744A>G
  hgvsp: ENSP00000331324.4:p.Tyr915Cys
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3143A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3071A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1329A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3071A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2789A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2789A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr915Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

16-68225328-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225328
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225328
    reference: chr 16
allele count: 6
allele frequency: 4.942013705851344e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2756A>T
  hgvsp: ENSP00000300659.5:p.His919Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2801A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2801A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2756A>T
  hgvsp: ENSP00000331324.4:p.His919Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2709A>T
  hgvsp: ENSP00000456120.1:p.His904Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2751A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2709A>T
  hgvsp: ENSP00000456379.1:p.His904Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3155A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3083A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2714A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2756A>T
  hgvsp: ENSP00000264008.6:p.His919Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3083A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3083A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1341A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2780A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2714A>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2756A>T
  hgvsp: ENSP00000460533.1:p.His919Leu
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His919Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-68225342-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225342
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225342
    reference: chr 16
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3169A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2815A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3097A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3097A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2770A>C
  hgvsp: ENSP00000264008.6:p.Thr924Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1355A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2723A>C
  hgvsp: ENSP00000456120.1:p.Thr909Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2765A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2770A>C
  hgvsp: ENSP00000331324.4:p.Thr924Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2723A>C
  hgvsp: ENSP00000456379.1:p.Thr909Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2770A>C
  hgvsp: ENSP00000460533.1:p.Thr924Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2770A>C
  hgvsp: ENSP00000300659.5:p.Thr924Pro
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3097A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2728A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2794A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2815A>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2728A>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7908
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr924Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

16-68225348-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225348
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225348
    reference: chr 16
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1361G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2776G>T
  hgvsp: ENSP00000300659.5:p.Ala926Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2729G>T
  hgvsp: ENSP00000456379.1:p.Ala911Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2776G>T
  hgvsp: ENSP00000460533.1:p.Ala926Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3103G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2771G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2800G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3175G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3103G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2734G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2776G>T
  hgvsp: ENSP00000264008.6:p.Ala926Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2776G>T
  hgvsp: ENSP00000331324.4:p.Ala926Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2821G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2734G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2729G>T
  hgvsp: ENSP00000456120.1:p.Ala911Ser
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3103G>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2821G>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala926Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/16-68225349-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225349
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225349
    reference: chr 16
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1362C>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2777C>A
  hgvsp: ENSP00000264008.6:p.Ala926Asp
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2730C>A
  hgvsp: ENSP00000456379.1:p.Ala911Asp
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2730C>A
  hgvsp: ENSP00000456120.1:p.Ala911Asp
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2735C>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3104C>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2777C>A
  hgvsp: ENSP00000300659.5:p.Ala926Asp
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2777C>A
  hgvsp: ENSP00000331324.4:p.Ala926Asp
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2735C>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2772C>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2822C>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3104C>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3104C>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2777C>A
  hgvsp: ENSP00000460533.1:p.Ala926Asp
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2801C>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3176C>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2822C>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala926Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS

16-68225349-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225349
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225349
    reference: chr 16
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2730C>T
  hgvsp: ENSP00000456379.1:p.Ala911Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2777C>T
  hgvsp: ENSP00000264008.6:p.Ala926Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2801C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2822C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2772C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3104C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2777C>T
  hgvsp: ENSP00000300659.5:p.Ala926Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2777C>T
  hgvsp: ENSP00000331324.4:p.Ala926Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2735C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2730C>T
  hgvsp: ENSP00000456120.1:p.Ala911Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2822C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3104C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2777C>T
  hgvsp: ENSP00000460533.1:p.Ala926Val
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3104C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2735C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3176C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1362C>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10150
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala926Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

16-68225355-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225355
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225355
    reference: chr 16
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2783C>T
  hgvsp: ENSP00000460533.1:p.Pro928Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2828C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2736C>T
  hgvsp: ENSP00000456120.1:p.Pro913Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3110C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2736C>T
  hgvsp: ENSP00000456379.1:p.Pro913Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2783C>T
  hgvsp: ENSP00000264008.6:p.Pro928Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2783C>T
  hgvsp: ENSP00000300659.5:p.Pro928Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2783C>T
  hgvsp: ENSP00000331324.4:p.Pro928Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3110C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3110C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2741C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2778C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2741C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1368C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3182C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2828C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2807C>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10152
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro928Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-68225357-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225357
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225357
    reference: chr 16
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2830G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2785G>A
  hgvsp: ENSP00000264008.6:p.Ala929Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3112G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1370G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2809G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2785G>A
  hgvsp: ENSP00000331324.4:p.Ala929Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3112G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2830G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2743G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2738G>A
  hgvsp: ENSP00000456379.1:p.Ala914Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2743G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2785G>A
  hgvsp: ENSP00000460533.1:p.Ala929Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2785G>A
  hgvsp: ENSP00000300659.5:p.Ala929Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2738G>A
  hgvsp: ENSP00000456120.1:p.Ala914Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3112G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2780G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3184G>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala929Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

16-68225360-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225360
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225360
    reference: chr 16
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2833G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2741G>A
  hgvsp: ENSP00000456120.1:p.Ala915Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3115G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2812G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2788G>A
  hgvsp: ENSP00000264008.6:p.Ala930Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3115G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3115G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2788G>A
  hgvsp: ENSP00000300659.5:p.Ala930Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2788G>A
  hgvsp: ENSP00000331324.4:p.Ala930Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2746G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3187G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2741G>A
  hgvsp: ENSP00000456379.1:p.Ala915Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2833G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2783G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2746G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2788G>A
  hgvsp: ENSP00000460533.1:p.Ala930Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1373G>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala930Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

16-68225363-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225363
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225363
    reference: chr 16
allele count: 3
allele frequency: 2.471210398853358e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2791T>A
  hgvsp: ENSP00000460533.1:p.Ser931Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2786T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3190T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3118T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2749T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2744T>A
  hgvsp: ENSP00000456120.1:p.Ser916Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2791T>A
  hgvsp: ENSP00000331324.4:p.Ser931Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2836T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3118T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3118T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2749T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2791T>A
  hgvsp: ENSP00000300659.5:p.Ser931Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1376T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2744T>A
  hgvsp: ENSP00000456379.1:p.Ser916Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2791T>A
  hgvsp: ENSP00000264008.6:p.Ser931Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2815T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2836T>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser931Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

16-68225371-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225371
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225371
    reference: chr 16
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3126C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2752C>T
  hgvsp: ENST00000570212.1:c.2752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2823C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3126C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2799C>T
  hgvsp: ENST00000329524.4:c.2799C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2799C>T
  hgvsp: ENST00000346183.3:c.2799C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3126C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2799C>T
  hgvsp: ENST00000349223.5:c.2799C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1384C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2844C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2757C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3198C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2799C>T
  hgvsp: ENST00000575270.1:c.2799C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2844C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2752C>T
  hgvsp: ENST00000562926.1:c.2752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2757C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2794C>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro933Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

16-68225379-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225379
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225379
    reference: chr 16
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2802G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2807G>C
  hgvsp: ENSP00000264008.6:p.Ser936Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2765G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2807G>C
  hgvsp: ENSP00000460533.1:p.Ser936Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3206G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3134G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2807G>C
  hgvsp: ENSP00000331324.4:p.Ser936Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2831G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2760G>C
  hgvsp: ENSP00000456379.1:p.Ser921Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2807G>C
  hgvsp: ENSP00000300659.5:p.Ser936Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2760G>C
  hgvsp: ENSP00000456120.1:p.Ser921Thr
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2852G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3134G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2765G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3134G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1392G>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2852G>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10159
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser936Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

16-68225385-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225385
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225385
    reference: chr 16
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2813C>T
  hgvsp: ENSP00000300659.5:p.Pro938Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3212C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3140C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2813C>T
  hgvsp: ENSP00000460533.1:p.Pro938Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2837C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3140C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1398C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2813C>T
  hgvsp: ENSP00000264008.6:p.Pro938Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2766C>T
  hgvsp: ENSP00000456120.1:p.Pro923Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2766C>T
  hgvsp: ENSP00000456379.1:p.Pro923Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2858C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2813C>T
  hgvsp: ENSP00000331324.4:p.Pro938Leu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2858C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2808C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3140C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2771C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2771C>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15483
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro938Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

16-68225386-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225386
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225386
    reference: chr 16
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2767G>A
  hgvsp: ENST00000562926.1:c.2767G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2838G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1399G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2772G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2814G>A
  hgvsp: ENST00000349223.5:c.2814G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2767G>A
  hgvsp: ENST00000570212.1:c.2767G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2814G>A
  hgvsp: ENST00000346183.3:c.2814G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3141G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2859G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3141G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2814G>A
  hgvsp: ENST00000575270.1:c.2814G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2809G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2772G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3213G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2814G>A
  hgvsp: ENST00000329524.4:c.2814G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3141G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2859G>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro938Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

16-68225389-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225389
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225389
    reference: chr 16
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2841T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2817T>C
  hgvsp: ENST00000329524.4:c.2817T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3216T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2812T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2770T>C
  hgvsp: ENST00000562926.1:c.2770T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1402T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2775T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3144T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2817T>C
  hgvsp: ENST00000346183.3:c.2817T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2817T>C
  hgvsp: ENST00000349223.5:c.2817T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2862T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3144T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2862T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3144T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2770T>C
  hgvsp: ENST00000570212.1:c.2770T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2775T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2817T>C
  hgvsp: ENST00000575270.1:c.2817T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5450
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu939Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-68225394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225394
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225394
    reference: chr 16
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2867G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2775G>A
  hgvsp: ENSP00000456379.1:p.Gly926Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2775G>A
  hgvsp: ENSP00000456120.1:p.Gly926Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3149G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2846G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1407G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2867G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3149G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2822G>A
  hgvsp: ENSP00000264008.6:p.Gly941Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2822G>A
  hgvsp: ENSP00000460533.1:p.Gly941Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2822G>A
  hgvsp: ENSP00000331324.4:p.Gly941Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2780G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2822G>A
  hgvsp: ENSP00000300659.5:p.Gly941Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3221G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2780G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2817G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3149G>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15485
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly941Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

16-68225398-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225398
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225398
    reference: chr 16
allele count: 8
allele frequency: 6.589677270555675e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2784A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2850A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2784A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3225A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3153A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2826A>G
  hgvsp: ENST00000575270.1:c.2826A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2826A>G
  hgvsp: ENST00000349223.5:c.2826A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2826A>G
  hgvsp: ENST00000329524.4:c.2826A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2871A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2779A>G
  hgvsp: ENST00000562926.1:c.2779A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2871A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2779A>G
  hgvsp: ENST00000570212.1:c.2779A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2821A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3153A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3153A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2826A>G
  hgvsp: ENST00000346183.3:c.2826A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1411A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro942Pro
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ

16-68225399-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225399
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225399
    reference: chr 16
allele count: 6
allele frequency: 4.942095118857387e-5
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2827C>G
  hgvsp: ENSP00000264008.6:p.Pro943Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2827C>G
  hgvsp: ENSP00000300659.5:p.Pro943Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2780C>G
  hgvsp: ENSP00000456379.1:p.Pro928Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2780C>G
  hgvsp: ENSP00000456120.1:p.Pro928Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2785C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2827C>G
  hgvsp: ENSP00000460533.1:p.Pro943Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3154C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2827C>G
  hgvsp: ENSP00000331324.4:p.Pro943Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2872C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3154C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2785C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1412C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2851C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3226C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2872C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2822C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3154C>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro943Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

16-68225401-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225401
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225401
    reference: chr 16
allele count: 411
allele frequency: 3.385335156417311e-3
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2874A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2829A>G
  hgvsp: ENST00000329524.4:c.2829A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2824A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2782A>G
  hgvsp: ENST00000570212.1:c.2782A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2874A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3156A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3228A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2829A>G
  hgvsp: ENST00000346183.3:c.2829A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2853A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1414A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2787A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3156A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3156A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2829A>G
  hgvsp: ENST00000575270.1:c.2829A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2782A>G
  hgvsp: ENST00000562926.1:c.2782A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2829A>G
  hgvsp: ENST00000349223.5:c.2829A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2787A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Pro943Pro
num of homozygotes: 7
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

16-68225404-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225404
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225404
    reference: chr 16
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3159T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2785T>A
  hgvsp: ENST00000562926.1:c.2785T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2832T>A
  hgvsp: ENST00000349223.5:c.2832T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1417T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2832T>A
  hgvsp: ENST00000346183.3:c.2832T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2832T>A
  hgvsp: ENST00000575270.1:c.2832T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2790T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2785T>A
  hgvsp: ENST00000570212.1:c.2785T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3231T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2877T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3159T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2832T>A
  hgvsp: ENST00000329524.4:c.2832T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2877T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2856T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2827T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2790T>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3159T>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser944Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum

16-68225408-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225408
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225408
    reference: chr 16
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2789C>G
  hgvsp: ENSP00000456120.1:p.Gln931Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3163C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2794C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1421C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2836C>G
  hgvsp: ENSP00000264008.6:p.Gln946Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2881C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2794C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2831C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2836C>G
  hgvsp: ENSP00000300659.5:p.Gln946Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2836C>G
  hgvsp: ENSP00000331324.4:p.Gln946Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2836C>G
  hgvsp: ENSP00000460533.1:p.Gln946Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2789C>G
  hgvsp: ENSP00000456379.1:p.Gln931Glu
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2881C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3235C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3163C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2860C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3163C>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln946Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-68225417-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225417
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225417
    reference: chr 16
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2803C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2845C>G
  hgvsp: ENSP00000331324.4:p.Pro949Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3172C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2869C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2845C>G
  hgvsp: ENSP00000264008.6:p.Pro949Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2890C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2798C>G
  hgvsp: ENSP00000456120.1:p.Pro934Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2845C>G
  hgvsp: ENSP00000300659.5:p.Pro949Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3172C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2840C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2798C>G
  hgvsp: ENSP00000456379.1:p.Pro934Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3244C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1430C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3172C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2845C>G
  hgvsp: ENSP00000460533.1:p.Pro949Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2890C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2803C>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro949Ala
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-68225425-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225425
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225425
    reference: chr 16
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2877T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3180T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2806T>C
  hgvsp: ENST00000562926.1:c.2806T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2853T>C
  hgvsp: ENST00000329524.4:c.2853T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1438T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2853T>C
  hgvsp: ENST00000349223.5:c.2853T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3180T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2811T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2898T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2806T>C
  hgvsp: ENST00000570212.1:c.2806T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2853T>C
  hgvsp: ENST00000346183.3:c.2853T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2898T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2853T>C
  hgvsp: ENST00000575270.1:c.2853T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3180T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2848T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2811T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3252T>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7954
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro951Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

16-68225431-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225431
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225431
    reference: chr 16
allele count: 33
allele frequency: 2.718107538218239e-4
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2859A>G
  hgvsp: ENST00000329524.4:c.2859A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2859A>G
  hgvsp: ENST00000575270.1:c.2859A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1444A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2817A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2859A>G
  hgvsp: ENST00000346183.3:c.2859A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2904A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3258A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3186A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2859A>G
  hgvsp: ENST00000349223.5:c.2859A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2854A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3186A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2883A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2904A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2812A>G
  hgvsp: ENST00000570212.1:c.2812A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2812A>G
  hgvsp: ENST00000562926.1:c.2812A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2817A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3186A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
hgvs: p.Gln953Gln
num of homozygotes: 1
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

16-68225434-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225434
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225434
    reference: chr 16
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3189T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2907T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2815T>C
  hgvsp: ENST00000562926.1:c.2815T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3261T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2862T>C
  hgvsp: ENST00000349223.5:c.2862T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2820T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3189T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3189T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2862T>C
  hgvsp: ENST00000346183.3:c.2862T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2862T>C
  hgvsp: ENST00000329524.4:c.2862T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2907T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2862T>C
  hgvsp: ENST00000575270.1:c.2862T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2815T>C
  hgvsp: ENST00000570212.1:c.2815T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1447T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2820T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2857T>C
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2886T>C
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10241
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser954Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

16-68225435-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225435
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225435
    reference: chr 16
allele count: 33
allele frequency: 2.718107538218239e-4
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2863C>G
  hgvsp: ENSP00000331324.4:p.Pro955Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2821C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1448C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2858C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2908C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2816C>G
  hgvsp: ENSP00000456120.1:p.Pro940Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2908C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2821C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2863C>G
  hgvsp: ENSP00000460533.1:p.Pro955Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3190C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2863C>G
  hgvsp: ENSP00000300659.5:p.Pro955Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2863C>G
  hgvsp: ENSP00000264008.6:p.Pro955Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3190C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2816C>G
  hgvsp: ENSP00000456379.1:p.Pro940Ala
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3262C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2887C>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3190C>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro955Ala
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

16-68225450-G-GCCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225450
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225453
    reference: chr 16
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: GCCT
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2880_2882dupCTC
  hgvsp: ENSP00000264008.6:p.Ser961dup
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2833_2835dupCTC
  hgvsp: ENSP00000456379.1:p.Ser946dup
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1465_*1467dupCTC
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2880_2882dupCTC
  hgvsp: ENSP00000460533.1:p.Ser961dup
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3207_3209dupCTC
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2880_2882dupCTC
  hgvsp: ENSP00000331324.4:p.Ser961dup
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3207_3209dupCTC
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2838_2840dupCTC
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2925_2927dupCTC
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2833_2835dupCTC
  hgvsp: ENSP00000456120.1:p.Ser946dup
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3279_3281dupCTC
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2925_2927dupCTC
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3207_3209dupCTC
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2880_2882dupCTC
  hgvsp: ENSP00000300659.5:p.Ser961dup
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2875_2877dupCTC
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2904_2906dupCTC
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2838_2840dupCTC
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 5465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser961dup
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

16-68225455-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225455
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225455
    reference: chr 16
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2841A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2883A>G
  hgvsp: ENST00000346183.3:c.2883A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3282A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2883A>G
  hgvsp: ENST00000575270.1:c.2883A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2841A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2883A>G
  hgvsp: ENST00000349223.5:c.2883A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2883A>G
  hgvsp: ENST00000329524.4:c.2883A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2836A>G
  hgvsp: ENST00000570212.1:c.2836A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3210A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2928A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2836A>G
  hgvsp: ENST00000562926.1:c.2836A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2928A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2878A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3210A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2907A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3210A>G
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1468A>G
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5464
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser961Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

16-68225461-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225461
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225461
    reference: chr 16
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3288G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2889G>A
  hgvsp: ENST00000346183.3:c.2889G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1474G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2889G>A
  hgvsp: ENST00000329524.4:c.2889G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2847G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2934G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2842G>A
  hgvsp: ENST00000562926.1:c.2842G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3216G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3216G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2934G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2847G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2889G>A
  hgvsp: ENST00000349223.5:c.2889G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2842G>A
  hgvsp: ENST00000570212.1:c.2842G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2889G>A
  hgvsp: ENST00000575270.1:c.2889G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3216G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2884G>A
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2913G>A
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro963Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS

16-68225472-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68225472
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 68225472
    reference: chr 16
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000445670
  ensembl transcript: ENST00000539828
  gene symbol: NFATC3
  hgvsc: ENST00000539828.2:c.*1485C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000567152
  gene symbol: NFATC3
  hgvsc: ENST00000567152.1:n.2858C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000264008
  ensembl transcript: ENST00000349223
  gene symbol: NFATC3
  hgvsc: ENST00000349223.5:c.2900C>T
  hgvsp: ENSP00000264008.6:p.Thr967Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000566301
  gene symbol: NFATC3
  hgvsc: ENST00000566301.1:n.2945C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000569766
  gene symbol: NFATC3
  hgvsc: ENST00000569766.1:n.3227C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456120
  ensembl transcript: ENST00000562926
  gene symbol: NFATC3
  hgvsc: ENST00000562926.1:c.2853C>T
  hgvsp: ENSP00000456120.1:p.Thr952Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000460533
  ensembl transcript: ENST00000575270
  gene symbol: NFATC3
  hgvsc: ENST00000575270.1:c.2900C>T
  hgvsp: ENSP00000460533.1:p.Thr967Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000331324
  ensembl transcript: ENST00000329524
  gene symbol: NFATC3
  hgvsc: ENST00000329524.4:c.2900C>T
  hgvsp: ENSP00000331324.4:p.Thr967Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000300659
  ensembl transcript: ENST00000346183
  gene symbol: NFATC3
  hgvsc: ENST00000346183.3:c.2900C>T
  hgvsp: ENSP00000300659.5:p.Thr967Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000379165
  gene symbol: NFATC3
  hgvsc: ENST00000379165.4:n.2924C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072736
  ensembl protein: ENSP00000456379
  ensembl transcript: ENST00000570212
  gene symbol: NFATC3
  hgvsc: ENST00000570212.1:c.2853C>T
  hgvsp: ENSP00000456379.1:p.Thr952Ile
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000549350
  gene symbol: NFATC3
  hgvsc: ENST00000549350.1:n.2945C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000535127
  gene symbol: NFATC3
  hgvsc: ENST00000535127.2:n.3299C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563288
  gene symbol: NFATC3
  hgvsc: ENST00000563288.1:n.2895C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563796
  gene symbol: NFATC3
  hgvsc: ENST00000563796.1:n.2858C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000553077
  gene symbol: NFATC3
  hgvsc: ENST00000553077.1:n.3227C>T
  variant of: http://identifiers.org/hgnc/7777
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072736
  ensembl transcript: ENST00000563319
  gene symbol: NFATC3
  hgvsc: ENST00000563319.1:n.3227C>T
  variant of: http://identifiers.org/hgnc/7777
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr967Ile
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 7916
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12203
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1023
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 705
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1908
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 476
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4107
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2650
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20348
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17319
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4497
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.59e-1

QD
type: SiteQuality
SIO_000300: 1.935e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.35e-1

DP
type: SiteQuality
SIO_000300: 2.057283e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

MQ
type: SiteQuality
SIO_000300: 6.053e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

GenotypeDepth
all individuals: 9
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 155
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3409
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1024
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 329
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 15746
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 404
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 271
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 705
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1908
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2653
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20343
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6015
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17322
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4107
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2155
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4501
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
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FS
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VQSLOD
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MQ
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MQ
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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VQSLOD
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MQRankSum
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ReadPosRankSum
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DP
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MQ
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FS
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Other
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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FS
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MQ
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InbreedingCoeff
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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African
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European (Finnish)
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East Asian
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BaseQRankSum
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MQ
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FS
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QD
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DP
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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African
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East Asian
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European (Non-Finnish)
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South Asian
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FS
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VQSLOD
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DP
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MQRankSum
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MQ
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QD
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European (Finnish)
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South Asian
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MQ
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DP
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VQSLOD
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QD
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GenotypeQuality
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East Asian
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FS
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MQ
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VQSLOD
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DP
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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DP
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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num of homozygotes: 0

Other
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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QD
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VQSLOD
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ReadPosRankSum
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DP
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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South Asian
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Other
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66740
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South Asian
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Latino
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Other
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African
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East Asian
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European (Finnish)
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InbreedingCoeff
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DP
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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FS
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VQSLOD
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QD
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Latino
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Other
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European (Non-Finnish)
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European (Finnish)
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African
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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MQ
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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Other
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South Asian
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MQ
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ClippingRankSum
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QD
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InbreedingCoeff
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MQRankSum
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DP
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 17

European (Non-Finnish)
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South Asian
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Latino
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African
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Other
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East Asian
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European (Finnish)
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MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
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FS
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VQSLOD
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QD
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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MQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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European (Finnish)
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African
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ReadPosRankSum
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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QD
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ReadPosRankSum
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ClippingRankSum
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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European (Finnish)
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MQ
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ClippingRankSum
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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DP
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QD
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ReadPosRankSum
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European (Non-Finnish)
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African
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Latino
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East Asian
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South Asian
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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QD
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FS
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DP
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East Asian
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VQSLOD
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QD
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InbreedingCoeff
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DP
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FS
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MQ
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ReadPosRankSum
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African
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East Asian
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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FS
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DP
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ReadPosRankSum
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Latino
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European (Finnish)
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East Asian
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VQSLOD
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MQRankSum
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QD
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FS
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MQ
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MQ
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DP
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InbreedingCoeff
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VQSLOD
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VQSLOD
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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East Asian
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South Asian
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VQSLOD
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ReadPosRankSum
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DP
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MQRankSum
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BaseQRankSum
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FS
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MQ
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ClippingRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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African
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Latino
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Other
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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FS
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QD
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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South Asian
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Latino
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Other
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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MQRankSum
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FS
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MQ
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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Other
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South Asian
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East Asian
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African
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QD
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InbreedingCoeff
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FS
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DP
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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MQRankSum
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East Asian
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DP
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VQSLOD
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East Asian
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African
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South Asian
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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DP
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MQ
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FS
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QD
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InbreedingCoeff
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GenotypeQuality
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East Asian
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African
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MQ
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DP
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QD
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VQSLOD
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African
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DP
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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South Asian
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European (Non-Finnish)
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East Asian
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Other
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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FS
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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African
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South Asian
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East Asian
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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VQSLOD
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QD
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FS
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MQ
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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African
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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FS
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MQ
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ReadPosRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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FS
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DP
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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East Asian
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Other
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South Asian
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European (Non-Finnish)
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QD
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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East Asian
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South Asian
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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QD
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DP
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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QD
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ClippingRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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South Asian
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African
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Other
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European (Non-Finnish)
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FS
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InbreedingCoeff
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MQRankSum
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DP
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VQSLOD
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ClippingRankSum
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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VQSLOD
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MQRankSum
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FS
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QD
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ReadPosRankSum
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MQ
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ClippingRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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East Asian
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African
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South Asian
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European (Finnish)
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FS
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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MQ
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African
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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DP
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MQRankSum
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FS
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MQ
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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Other
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South Asian
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African
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European (Finnish)
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FS
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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DP
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SIO_000300: 2.064108e6

BaseQRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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FS
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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DP
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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QD
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FS
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 5.502e1

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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66740
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East Asian
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South Asian
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European (Finnish)
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Other
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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DP
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ClippingRankSum
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MQ
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 5.993586862057598e-5
allele num: 66738
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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South Asian
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Other
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DP
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ClippingRankSum
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MQ
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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