16-69689742-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69689742
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69689740
    reference: chr 16
allele count: 1
allele frequency: 8.466396870819716e-6
allele num: 118114
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1196+41_1196+42delTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.914+41_914+42delTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1142+41_1142+42delTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*958+41_*958+42delTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+8673_36+8674delTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.914+41_914+42delTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*539+41_*539+42delTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+41_384+42delTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1196+41_1196+42delTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.914+41_914+42delTT
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13357
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10128
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1458
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: CTT
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

16-69689745-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69689745
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69689745
    reference: chr 16
allele count: 2
allele frequency: 1.695576241585703e-5
allele num: 117954
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.914+43G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1196+43G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1142+43G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*958+43G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.914+43G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+43G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+8675G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1196+43G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*539+43G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.914+43G>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10324
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2705
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10127
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3759
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

16-69689746-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69689746
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69689746
    reference: chr 16
allele count: 25
allele frequency: 2.118967300096625e-4
allele num: 117982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*539+44T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.914+44T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+8676T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+44T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*958+44T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1142+44T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.914+44T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1196+44T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.914+44T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1196+44T>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10229
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6324
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10269
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2927
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

16-69689746-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69689746
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69689746
    reference: chr 16
allele count: 11
allele frequency: 9.32345612042515e-5
allele num: 117982
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.914+44T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1196+44T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*958+44T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+44T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+8676T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.914+44T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.914+44T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1142+44T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*539+44T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1196+44T>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6324
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10269
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10149
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

16-69689748-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69689748
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69689748
    reference: chr 16
allele count: 1
allele frequency: 8.499065102838687e-6
allele num: 117660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*958+46T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.914+46T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.914+46T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+46T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.914+46T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+8678T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*539+46T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1196+46T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1196+46T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1142+46T>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

16-69689749-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69689749
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69689749
    reference: chr 16
allele count: 1
allele frequency: 8.499787505312367e-6
allele num: 117650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+47T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1142+47T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+8679T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1196+47T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.914+47T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.914+47T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*958+47T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1196+47T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.914+47T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*539+47T>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6392
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

16-69689752-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69689752
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69689752
    reference: chr 16
allele count: 1
allele frequency: 8.519338899301415e-6
allele num: 117380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.914+50G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1196+50G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+50G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1142+50G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*958+50G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1196+50G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.914+50G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*539+50G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.914+50G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+8682G>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 11689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5912
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9750
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1670
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

16-69689753-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69689753
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69689753
    reference: chr 16
allele count: 1
allele frequency: 8.568539749455898e-6
allele num: 116706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1196+51C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*958+51C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+8683C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.914+51C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+51C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1196+51C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.914+51C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1142+51C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*539+51C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.914+51C>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11673
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11657
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5894
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2284
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2908
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

16-69693579-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693579
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693579
    reference: chr 16
allele count: 9
allele frequency: 7.834261838440112e-5
allele num: 114880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915-51A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12509A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143-51A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197-51A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959-51A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197-51A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540-51A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915-51A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3877A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915-51A>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6503
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8864
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3572
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

16-69693584-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693584
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693584
    reference: chr 16
allele count: 2
allele frequency: 1.739917179942235e-5
allele num: 114948
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540-46A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915-46A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3882A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197-46A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915-46A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959-46A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12514A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197-46A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143-46A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915-46A>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7843
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7759
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3595
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1533
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

16-69693588-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693588
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693588
    reference: chr 16
allele count: 5
allele frequency: 4.347070074769605e-5
allele num: 115020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915-42A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959-42A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197-42A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915-42A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3886A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12518A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540-42A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915-42A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197-42A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143-42A>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4829
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD

16-69693590-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693590
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693590
    reference: chr 16
allele count: 1
allele frequency: 8.687191604698033e-6
allele num: 115112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3888A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915-40A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12520A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197-40A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197-40A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540-40A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959-40A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143-40A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915-40A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915-40A>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4074
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

16-69693602-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693602
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693602
    reference: chr 16
allele count: 2
allele frequency: 1.723484195649926e-5
allele num: 116044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959-28C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143-28C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915-28C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12532C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540-28C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197-28C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3900C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915-28C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915-28C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197-28C>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3649
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5127
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

16-69693607-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693607
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693607
    reference: chr 16
allele count: 1
allele frequency: 8.573976267233693e-6
allele num: 116632
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197-23T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197-23T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959-23T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3905T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915-23T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915-23T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12537T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143-23T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540-23T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915-23T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20597
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-69693608-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693608
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693608
    reference: chr 16
allele count: 1
allele frequency: 8.563550105331666e-6
allele num: 116774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12538A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915-22A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143-22A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915-22A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915-22A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959-22A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197-22A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540-22A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3906A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197-22A>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7833
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2226
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

16-69693612-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693612
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693613
    reference: chr 16
allele count: 29
allele frequency: 2.481516976998905e-4
allele num: 116864
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915-10dupT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540-10dupT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915-10dupT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3918dupT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959-10dupT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197-10dupT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915-10dupT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197-10dupT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12550dupT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143-10dupT
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12057
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2571
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20603
  bin: 9.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 1877
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

16-69693612-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693612
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693611
    reference: chr 16
allele count: 10
allele frequency: 8.556955093099671e-5
allele num: 116864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12550delT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959-10delT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540-10delT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915-10delT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3918delT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915-10delT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197-10delT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197-10delT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915-10delT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143-10delT
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7923
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1877
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5106
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: AT
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

16-69693614-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693614
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693614
    reference: chr 16
allele count: 15
allele frequency: 1.27607445469085e-4
allele num: 117548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12544T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915-16T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197-16T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915-16T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3912T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143-16T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540-16T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915-16T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959-16T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197-16T>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10115
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10030
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

16-69693625-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693625
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693625
    reference: chr 16
allele count: 6
allele frequency: 5.006592012816876e-5
allele num: 119842
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197-5A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197-5A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12555A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915-5A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915-5A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540-5A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959-5A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3923A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143-5A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915-5A>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7956
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10117
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 1
hgvs: c.1197-5A>T
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum

16-69693630-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693630
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693630
    reference: chr 16
allele count: 1
allele frequency: 8.297791128001726e-6
allele num: 120514
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915G>A
  hgvsp: ENST00000393742.2:c.915G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143G>A
  hgvsp: ENST00000354436.2:c.1143G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197G>A
  hgvsp: ENST00000567239.1:c.1197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915G>A
  hgvsp: ENST00000566899.1:c.915G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197G>A
  hgvsp: ENST00000432919.1:c.1197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3928G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915G>A
  hgvsp: ENST00000349945.1:c.915G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12560G>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1197G>A
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

16-69693630-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693630
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693630
    reference: chr 16
allele count: 1
allele frequency: 8.297791128001726e-6
allele num: 120514
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1197G>C
  hgvsp: ENST00000432919.1:c.1197G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*540G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1197G>C
  hgvsp: ENST00000567239.1:c.1197G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.915G>C
  hgvsp: ENST00000393742.2:c.915G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12560G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.915G>C
  hgvsp: ENST00000566899.1:c.915G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.915G>C
  hgvsp: ENST00000349945.1:c.915G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1143G>C
  hgvsp: ENST00000354436.2:c.1143G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*959G>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3928G>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1197G>C
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

16-69693639-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693639
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693639
    reference: chr 16
allele count: 7
allele frequency: 5.788376939106274e-5
allele num: 120932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1152C>T
  hgvsp: ENST00000354436.2:c.1152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.924C>T
  hgvsp: ENST00000393742.2:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3937C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*549C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1206C>T
  hgvsp: ENST00000567239.1:c.1206C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12569C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.924C>T
  hgvsp: ENST00000349945.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1206C>T
  hgvsp: ENST00000432919.1:c.1206C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*968C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.924C>T
  hgvsp: ENST00000566899.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys402Cys
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

16-69693640-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693640
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693640
    reference: chr 16
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1207G>A
  hgvsp: ENSP00000396538.1:p.Val403Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.925G>A
  hgvsp: ENSP00000377343.2:p.Val309Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*550G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*969G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.925G>A
  hgvsp: ENSP00000338806.2:p.Val309Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.925G>A
  hgvsp: ENSP00000455628.1:p.Val309Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3938G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12570G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1207G>A
  hgvsp: ENSP00000457593.1:p.Val403Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1153G>A
  hgvsp: ENSP00000346420.2:p.Val385Ile
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5541
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val403Ile
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: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

16-69693649-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693649
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693649
    reference: chr 16
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.934T>C
  hgvsp: ENST00000349945.1:c.934T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.934T>C
  hgvsp: ENST00000393742.2:c.934T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12579T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3947T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1162T>C
  hgvsp: ENST00000354436.2:c.1162T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*559T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.934T>C
  hgvsp: ENST00000566899.1:c.934T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1216T>C
  hgvsp: ENST00000567239.1:c.1216T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1216T>C
  hgvsp: ENST00000432919.1:c.1216T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*978T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu406Leu
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP

16-69693663-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693663
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693663
    reference: chr 16
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.948T>C
  hgvsp: ENST00000393742.2:c.948T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12593T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1230T>C
  hgvsp: ENST00000567239.1:c.1230T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.948T>C
  hgvsp: ENST00000349945.1:c.948T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1176T>C
  hgvsp: ENST00000354436.2:c.1176T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*573T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*992T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.948T>C
  hgvsp: ENST00000566899.1:c.948T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1230T>C
  hgvsp: ENST00000432919.1:c.1230T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3961T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20669
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asn410Asn
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

16-69693670-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693670
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693670
    reference: chr 16
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.955G>A
  hgvsp: ENSP00000455628.1:p.Val319Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1237G>A
  hgvsp: ENSP00000457593.1:p.Val413Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1183G>A
  hgvsp: ENSP00000346420.2:p.Val395Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3968G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.955G>A
  hgvsp: ENSP00000338806.2:p.Val319Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*580G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1237G>A
  hgvsp: ENSP00000396538.1:p.Val413Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.955G>A
  hgvsp: ENSP00000377343.2:p.Val319Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12600G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*999G>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val413Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

16-69693672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693672
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693672
    reference: chr 16
allele count: 25
allele frequency: 2.059817088242564e-4
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.957C>T
  hgvsp: ENST00000349945.1:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+3970C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1185C>T
  hgvsp: ENST00000354436.2:c.1185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.957C>T
  hgvsp: ENST00000393742.2:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*582C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1239C>T
  hgvsp: ENST00000567239.1:c.1239C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.957C>T
  hgvsp: ENST00000566899.1:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1001C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1239C>T
  hgvsp: ENST00000432919.1:c.1239C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12602C>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7960
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5571
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val413Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

16-69693712-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693712
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693712
    reference: chr 16
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1279A>G
  hgvsp: ENSP00000457593.1:p.Thr427Ala
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12642A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.997A>G
  hgvsp: ENSP00000455628.1:p.Thr333Ala
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1041A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1279A>G
  hgvsp: ENSP00000396538.1:p.Thr427Ala
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.997A>G
  hgvsp: ENSP00000377343.2:p.Thr333Ala
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1225A>G
  hgvsp: ENSP00000346420.2:p.Thr409Ala
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.997A>G
  hgvsp: ENSP00000338806.2:p.Thr333Ala
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4010A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*622A>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11011
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr427Ala
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

16-69693715-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693715
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693715
    reference: chr 16
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1282C>T
  hgvsp: ENSP00000396538.1:p.Arg428Cys
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1000C>T
  hgvsp: ENSP00000377343.2:p.Arg334Cys
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12645C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1000C>T
  hgvsp: ENSP00000455628.1:p.Arg334Cys
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4013C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1228C>T
  hgvsp: ENSP00000346420.2:p.Arg410Cys
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1044C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1282C>T
  hgvsp: ENSP00000457593.1:p.Arg428Cys
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1000C>T
  hgvsp: ENSP00000338806.2:p.Arg334Cys
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*625C>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2688
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg428Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

16-69693716-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693716
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693716
    reference: chr 16
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4014G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1283G>A
  hgvsp: ENSP00000396538.1:p.Arg428His
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1045G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1001G>A
  hgvsp: ENSP00000338806.2:p.Arg334His
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12646G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1229G>A
  hgvsp: ENSP00000346420.2:p.Arg410His
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1001G>A
  hgvsp: ENSP00000377343.2:p.Arg334His
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1283G>A
  hgvsp: ENSP00000457593.1:p.Arg428His
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1001G>A
  hgvsp: ENSP00000455628.1:p.Arg334His
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*626G>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4275
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg428His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

16-69693724-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693724
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693724
    reference: chr 16
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1009T>C
  hgvsp: ENST00000393742.2:c.1009T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1009T>C
  hgvsp: ENST00000566899.1:c.1009T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1237T>C
  hgvsp: ENST00000354436.2:c.1237T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1291T>C
  hgvsp: ENST00000432919.1:c.1291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1053T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1291T>C
  hgvsp: ENST00000567239.1:c.1291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1009T>C
  hgvsp: ENST00000349945.1:c.1009T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*634T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4022T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12654T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu431Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

16-69693739-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693739
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693739
    reference: chr 16
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12669A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1068A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1306A>G
  hgvsp: ENSP00000396538.1:p.Asn436Asp
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1306A>G
  hgvsp: ENSP00000457593.1:p.Asn436Asp
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1252A>G
  hgvsp: ENSP00000346420.2:p.Asn418Asp
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1024A>G
  hgvsp: ENSP00000338806.2:p.Asn342Asp
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1024A>G
  hgvsp: ENSP00000377343.2:p.Asn342Asp
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4037A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1024A>G
  hgvsp: ENSP00000455628.1:p.Asn342Asp
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*649A>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn436Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

16-69693747-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693747
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693747
    reference: chr 16
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1032G>A
  hgvsp: ENSP00000338806.2:p.Met344Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1032G>A
  hgvsp: ENSP00000455628.1:p.Met344Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*657G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4045G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1314G>A
  hgvsp: ENSP00000457593.1:p.Met438Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1260G>A
  hgvsp: ENSP00000346420.2:p.Met420Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1076G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1314G>A
  hgvsp: ENSP00000396538.1:p.Met438Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1032G>A
  hgvsp: ENSP00000377343.2:p.Met344Ile
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12677G>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Met438Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-69693748-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693748
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693748
    reference: chr 16
allele count: 3
allele frequency: 2.47133254250692e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12678A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1261A>C
  hgvsp: ENST00000354436.2:c.1261A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1315A>C
  hgvsp: ENST00000432919.1:c.1315A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1315A>C
  hgvsp: ENST00000567239.1:c.1315A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1033A>C
  hgvsp: ENST00000566899.1:c.1033A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1033A>C
  hgvsp: ENST00000393742.2:c.1033A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1077A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*658A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1033A>C
  hgvsp: ENST00000349945.1:c.1033A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4046A>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5802
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg439Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

16-69693759-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693759
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693759
    reference: chr 16
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1326C>T
  hgvsp: ENST00000432919.1:c.1326C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1088C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1326C>T
  hgvsp: ENST00000567239.1:c.1326C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12689C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1272C>T
  hgvsp: ENST00000354436.2:c.1272C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1044C>T
  hgvsp: ENST00000393742.2:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1044C>T
  hgvsp: ENST00000349945.1:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4057C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1044C>T
  hgvsp: ENST00000566899.1:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*669C>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly442Gly
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

16-69693778-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693778
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693778
    reference: chr 16
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1345A>T
  hgvsp: ENSP00000457593.1:p.Thr449Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1063A>T
  hgvsp: ENSP00000338806.2:p.Thr355Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1063A>T
  hgvsp: ENSP00000377343.2:p.Thr355Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12708A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1063A>T
  hgvsp: ENSP00000455628.1:p.Thr355Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1345A>T
  hgvsp: ENSP00000396538.1:p.Thr449Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*688A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1291A>T
  hgvsp: ENSP00000346420.2:p.Thr431Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4076A>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1107A>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2680
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr449Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

16-69693792-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693792
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693792
    reference: chr 16
allele count: 3
allele frequency: 2.478888136041381e-5
allele num: 121022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12722A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1077A>G
  hgvsp: ENST00000393742.2:c.1077A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1305A>G
  hgvsp: ENST00000354436.2:c.1305A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1359A>G
  hgvsp: ENST00000432919.1:c.1359A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1121A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1077A>G
  hgvsp: ENST00000349945.1:c.1077A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*702A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1359A>G
  hgvsp: ENST00000567239.1:c.1359A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1077A>G
  hgvsp: ENST00000566899.1:c.1077A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4090A>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13604
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro453Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

16-69693796-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693796
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693796
    reference: chr 16
allele count: 18
allele frequency: 1.488710611198412e-4
allele num: 120910
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1309T>C
  hgvsp: ENST00000354436.2:c.1309T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1363T>C
  hgvsp: ENST00000567239.1:c.1363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12726T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1125T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*706T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1081T>C
  hgvsp: ENST00000566899.1:c.1081T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1081T>C
  hgvsp: ENST00000349945.1:c.1081T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1081T>C
  hgvsp: ENST00000393742.2:c.1081T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1363T>C
  hgvsp: ENST00000432919.1:c.1363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4094T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5809
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7986
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4261
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu455Leu
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

16-69693818-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693818
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693818
    reference: chr 16
allele count: 2
allele frequency: 1.670983373715432e-5
allele num: 119690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1087+16C>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1087+16C>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1369+16C>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12748C>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*712+16C>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4116C>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1315+16C>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1369+16C>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1131+16C>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1087+16C>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

16-69693818-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693818
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693818
    reference: chr 16
allele count: 24
allele frequency: 2.005180048458518e-4
allele num: 119690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12748C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1369+16C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1087+16C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1087+16C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1131+16C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1087+16C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*712+16C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4116C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1369+16C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1315+16C>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7964
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11626
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5283
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

16-69693819-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693819
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693819
    reference: chr 16
allele count: 10
allele frequency: 8.357709987463435e-5
allele num: 119650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1087+17G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4117G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1315+17G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1369+17G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12749G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1087+17G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1087+17G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*712+17G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1131+17G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1369+17G>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10083
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11535
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10496
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2256
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

16-69693822-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693822
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693822
    reference: chr 16
allele count: 1
allele frequency: 8.369741709770836e-6
allele num: 119478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12752G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1087+20G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1315+20G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1087+20G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1369+20G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1131+20G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1087+20G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4120G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1369+20G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*712+20G>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20668
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

16-69693831-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693831
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693831
    reference: chr 16
allele count: 1
allele frequency: 8.405621679779436e-6
allele num: 118968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12761C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1087+29C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1369+29C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1087+29C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4129C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1087+29C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*712+29C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1315+29C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1131+29C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1369+29C>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4218
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

16-69693835-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693835
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693835
    reference: chr 16
allele count: 2
allele frequency: 1.683643404326963e-5
allele num: 118790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1087+33T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1087+33T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4133T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1315+33T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12765T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1369+33T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1087+33T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*712+33T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1131+33T>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1369+33T>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4217
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

16-69693835-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693835
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693835
    reference: chr 16
allele count: 7
allele frequency: 5.892751915144372e-5
allele num: 118790
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1315+33T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1087+33T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1087+33T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1369+33T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*712+33T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12765T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1131+33T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1369+33T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1087+33T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4133T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5163
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum

16-69693836-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693836
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693836
    reference: chr 16
allele count: 10
allele frequency: 8.421903687109434e-5
allele num: 118738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1087+34G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1131+34G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1369+34G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12766G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1087+34G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1087+34G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1315+34G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*712+34G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4134G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1369+34G>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9731
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9770
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2616
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/16-69693843-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693843
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693843
    reference: chr 16
allele count: 1
allele frequency: 8.490405841399219e-6
allele num: 117780
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1369+41C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1131+41C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1315+41C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1369+41C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4141C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12773C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1087+41C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*712+41C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1087+41C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1087+41C>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2547
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/16-69693847-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69693847
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69693847
    reference: chr 16
allele count: 2
allele frequency: 1.701953843011778e-5
allele num: 117512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1087+45C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1369+45C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.384+4145C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*712+45C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1131+45C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1315+45C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1369+45C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1087+45C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+12777C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1087+45C>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3694
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/16-69703835-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703835
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703835
    reference: chr 16
allele count: 2
allele frequency: 1.75404746452439e-5
allele num: 114022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.385-45A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1088-45A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1370-45A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1316-45A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1132-45A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22765A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1370-45A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1088-45A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1088-45A>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*713-45A>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4886
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2929
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13938
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2148
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

16-69703837-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703837
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703837
    reference: chr 16
allele count: 1
allele frequency: 8.774854776153454e-6
allele num: 113962
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1088-43G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*713-43G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1316-43G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1132-43G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.385-43G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1370-43G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1088-43G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1088-43G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1370-43G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22767G>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11194
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4191
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

16-69703846-GTTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703846
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703843
    reference: chr 16
allele count: 3
allele frequency: 2.624671916010499e-5
allele num: 114300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22782_36+22784delCTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1132-28_*1132-26delCTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.385-28_385-26delCTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1370-28_1370-26delCTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1088-28_1088-26delCTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1316-28_1316-26delCTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1088-28_1088-26delCTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1370-28_1370-26delCTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1088-28_1088-26delCTT
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*713-28_*713-26delCTT
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9616
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6381
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: GTTC
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

16-69703847-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703847
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703847
    reference: chr 16
allele count: 1
allele frequency: 8.743092956564315e-6
allele num: 114376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*713-33T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1370-33T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1370-33T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1316-33T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1088-33T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1088-33T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.385-33T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22777T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1088-33T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1132-33T>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9633
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD

16-69703854-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703854
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703854
    reference: chr 16
allele count: 1
allele frequency: 8.715204545850691e-6
allele num: 114742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1316-26T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1370-26T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22784T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1088-26T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.385-26T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1088-26T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1132-26T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*713-26T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1088-26T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1370-26T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12235
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-69703856-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703856
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703856
    reference: chr 16
allele count: 2
allele frequency: 1.740341106856944e-5
allele num: 114920
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1370-24T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.385-24T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22786T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1370-24T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1132-24T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1088-24T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1088-24T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1088-24T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1316-24T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*713-24T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3199
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14002
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

16-69703859-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703859
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703859
    reference: chr 16
allele count: 189
allele frequency: 1.6400270734628e-3
allele num: 115242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1132-21A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22789A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1088-21A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1370-21A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.385-21A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1088-21A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*713-21A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1316-21A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1370-21A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1088-21A>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 1.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 1.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 9941
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 12471
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 3.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15641
  bin: 2.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.25e1
  variant carriers: 1
num of homozygotes: 2
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-69703863-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703863
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703863
    reference: chr 16
allele count: 714
allele frequency: 6.180854931698956e-3
allele num: 115518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1132-17C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1316-17C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.385-17C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1088-17C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*713-17C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22793C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1088-17C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1370-17C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1088-17C>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1370-17C>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 12496
  bin: 2.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 3.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 3596
  bin: 4.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 4.75e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 15871
  bin: 2.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 10056
  bin: 3.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 6013
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4415
  bin: 8.25e1
  variant carriers: 3
num of homozygotes: 20
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

16-69703864-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703864
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703864
    reference: chr 16
allele count: 6
allele frequency: 5.184570717544587e-5
allele num: 115728
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*713-16T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1132-16T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.385-16T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1088-16T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1370-16T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22794T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1316-16T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1370-16T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1088-16T>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1088-16T>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16242
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6105
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

16-69703865-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703865
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703865
    reference: chr 16
allele count: 1
allele frequency: 8.633640115345432e-6
allele num: 115826
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1088-15T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1132-15T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1370-15T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1088-15T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*713-15T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1316-15T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22795T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1088-15T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1370-15T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.385-15T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4751
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16387
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

16-69703866-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703866
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703866
    reference: chr 16
allele count: 9
allele frequency: 7.764243072569792e-5
allele num: 115916
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1132-14A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1088-14A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*713-14A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1088-14A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1088-14A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.385-14A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1370-14A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1316-14A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22796A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1370-14A>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6128
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3172
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-69703903-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703903
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703903
    reference: chr 16
allele count: 3
allele frequency: 2.496297159213833e-5
allele num: 120178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1111A>G
  hgvsp: ENSP00000377343.2:p.Ile371Val
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1111A>G
  hgvsp: ENSP00000338806.2:p.Ile371Val
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*736A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.408A>G
  hgvsp: ENSP00000462061.1:p.Asn137Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1339A>G
  hgvsp: ENSP00000346420.2:p.Ile447Val
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1111A>G
  hgvsp: ENSP00000455628.1:p.Ile371Val
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1155A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22833A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1393A>G
  hgvsp: ENSP00000457593.1:p.Ile465Val
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1393A>G
  hgvsp: ENSP00000396538.1:p.Ile465Val
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile465Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS

16-69703919-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703919
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703919
    reference: chr 16
allele count: 2
allele frequency: 1.657138122462507e-5
allele num: 120690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1127T>C
  hgvsp: ENSP00000377343.2:p.Leu376Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*752T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1409T>C
  hgvsp: ENSP00000457593.1:p.Leu470Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1409T>C
  hgvsp: ENSP00000396538.1:p.Leu470Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1127T>C
  hgvsp: ENSP00000338806.2:p.Leu376Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1355T>C
  hgvsp: ENSP00000346420.2:p.Leu452Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1127T>C
  hgvsp: ENSP00000455628.1:p.Leu376Ser
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.424T>C
  hgvsp: ENST00000563474.2:c.424T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1171T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22849T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18451
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu470Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

16-69703922-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703922
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703922
    reference: chr 16
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1358A>G
  hgvsp: ENSP00000346420.2:p.His453Arg
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1130A>G
  hgvsp: ENSP00000338806.2:p.His377Arg
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1130A>G
  hgvsp: ENSP00000377343.2:p.His377Arg
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1130A>G
  hgvsp: ENSP00000455628.1:p.His377Arg
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1412A>G
  hgvsp: ENSP00000396538.1:p.His471Arg
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1412A>G
  hgvsp: ENSP00000457593.1:p.His471Arg
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.427A>G
  hgvsp: ENST00000563474.2:c.427A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*755A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1174A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22852A>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18473
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His471Arg
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

16-69703923-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703923
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703923
    reference: chr 16
allele count: 1
allele frequency: 8.27841981522567e-6
allele num: 120796
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1413T>C
  hgvsp: ENST00000432919.1:c.1413T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1131T>C
  hgvsp: ENST00000349945.1:c.1131T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.428T>C
  hgvsp: ENSP00000462061.1:p.Ter144GlnextTer21
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1131T>C
  hgvsp: ENST00000393742.2:c.1131T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1359T>C
  hgvsp: ENST00000354436.2:c.1359T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*756T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1413T>C
  hgvsp: ENST00000567239.1:c.1413T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1175T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1131T>C
  hgvsp: ENST00000566899.1:c.1131T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22853T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ter144GlnextTer21
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

16-69703935-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703935
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703935
    reference: chr 16
allele count: 1
allele frequency: 8.270204108637402e-6
allele num: 120916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1187G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1425G>A
  hgvsp: ENST00000567239.1:c.1425G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22865G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1143G>A
  hgvsp: ENST00000349945.1:c.1143G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1425G>A
  hgvsp: ENST00000432919.1:c.1425G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1143G>A
  hgvsp: ENST00000566899.1:c.1143G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.*10G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1143G>A
  hgvsp: ENST00000393742.2:c.1143G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1371G>A
  hgvsp: ENST00000354436.2:c.1371G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*768G>A
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10744
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6677
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val475Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

16-69703944-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703944
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703944
    reference: chr 16
allele count: 5
allele frequency: 4.132846208526888e-5
allele num: 120982
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1434A>G
  hgvsp: ENST00000567239.1:c.1434A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.*19A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1152A>G
  hgvsp: ENST00000349945.1:c.1152A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*777A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1380A>G
  hgvsp: ENST00000354436.2:c.1380A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1196A>G
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1152A>G
  hgvsp: ENST00000393742.2:c.1152A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1434A>G
  hgvsp: ENST00000432919.1:c.1434A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1152A>G
  hgvsp: ENST00000566899.1:c.1152A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22874A>G
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6656
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu478Glu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

16-69703945-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703945
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703945
    reference: chr 16
allele count: 4
allele frequency: 3.30611300294244e-5
allele num: 120988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1197G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1435G>A
  hgvsp: ENSP00000396538.1:p.Glu479Lys
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1153G>A
  hgvsp: ENSP00000338806.2:p.Glu385Lys
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.*20G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22875G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1435G>A
  hgvsp: ENSP00000457593.1:p.Glu479Lys
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1153G>A
  hgvsp: ENSP00000455628.1:p.Glu385Lys
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1381G>A
  hgvsp: ENSP00000346420.2:p.Glu461Lys
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*778G>A
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1153G>A
  hgvsp: ENSP00000377343.2:p.Glu385Lys
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18416
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10773
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu479Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

16-69703962-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703962
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703962
    reference: chr 16
allele count: 4
allele frequency: 3.305402680681574e-5
allele num: 121014
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1170C>T
  hgvsp: ENST00000566899.1:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1398C>T
  hgvsp: ENST00000354436.2:c.1398C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1452C>T
  hgvsp: ENST00000567239.1:c.1452C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.*37C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1170C>T
  hgvsp: ENST00000393742.2:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1170C>T
  hgvsp: ENST00000349945.1:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1452C>T
  hgvsp: ENST00000432919.1:c.1452C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1214C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22892C>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*795C>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14305
  bin: 9.75e1
  variant carriers: 4
hgvs: p.Ile484Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

16-69703974-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703974
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703974
    reference: chr 16
allele count: 2
allele frequency: 1.652919882973272e-5
allele num: 120998
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1182T>C
  hgvsp: ENST00000393742.2:c.1182T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1464T>C
  hgvsp: ENST00000567239.1:c.1464T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22904T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1464T>C
  hgvsp: ENST00000432919.1:c.1464T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1182T>C
  hgvsp: ENST00000566899.1:c.1182T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1226T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1182T>C
  hgvsp: ENST00000349945.1:c.1182T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1410T>C
  hgvsp: ENST00000354436.2:c.1410T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*807T>C
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.*49T>C
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe488Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
reference allele: T
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

16-69703977-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69703977
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 69703977
    reference: chr 16
allele count: 1
allele frequency: 8.267059076404159e-6
allele num: 120962
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000463214
  ensembl transcript: ENST00000565301
  gene symbol: NFAT5
  hgvsc: ENST00000565301.1:c.36+22907G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000457593
  ensembl transcript: ENST00000567239
  gene symbol: NFAT5
  hgvsc: ENST00000567239.1:c.1467G>T
  hgvsp: ENST00000567239.1:c.1467G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455628
  ensembl transcript: ENST00000566899
  gene symbol: NFAT5
  hgvsc: ENST00000566899.1:c.1185G>T
  hgvsp: ENST00000566899.1:c.1185G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000338806
  ensembl transcript: ENST00000349945
  gene symbol: NFAT5
  hgvsc: ENST00000349945.1:c.1185G>T
  hgvsp: ENST00000349945.1:c.1185G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000396538
  ensembl transcript: ENST00000432919
  gene symbol: NFAT5
  hgvsc: ENST00000432919.1:c.1467G>T
  hgvsp: ENST00000432919.1:c.1467G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000413126
  ensembl transcript: ENST00000426654
  gene symbol: NFAT5
  hgvsc: ENST00000426654.2:c.*1229G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000346420
  ensembl transcript: ENST00000354436
  gene symbol: NFAT5
  hgvsc: ENST00000354436.2:c.1413G>T
  hgvsp: ENST00000354436.2:c.1413G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000377343
  ensembl transcript: ENST00000393742
  gene symbol: NFAT5
  hgvsc: ENST00000393742.2:c.1185G>T
  hgvsp: ENST00000393742.2:c.1185G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000455115
  ensembl transcript: ENST00000567990
  gene symbol: NFAT5
  hgvsc: ENST00000567990.1:c.*810G>T
  variant of: http://identifiers.org/hgnc/7774
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000102908
  ensembl protein: ENSP00000462061
  ensembl transcript: ENST00000563474
  gene symbol: NFAT5
  hgvsc: ENST00000563474.2:c.*52G>T
  variant of: http://identifiers.org/hgnc/7774
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 1
hgvs: p.Leu489Leu
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 1776
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4450
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2954
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6934
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3766
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2706
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2147
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15659
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522533495736906e-5
allele num: 65680
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 1.173e1

DP
type: SiteQuality
SIO_000300: 1.795699e6

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.995e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.827e0

GenotypeQuality
all individuals: 291
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2625
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2910
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2931
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1792
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1531
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1269
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13552
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2592
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4431
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1774
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6732
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.046180090166931e-5
allele num: 65656
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.043e0

MQRankSum
type: SiteQuality
SIO_000300: -9.74e-1

DP
type: SiteQuality
SIO_000300: 1.781825e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

QD
type: SiteQuality
SIO_000300: 1.576e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.76e-1

GenotypeQuality
all individuals: 13818
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2936
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2593
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2621
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6727
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1537
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4426
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10149
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 1261
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2700
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3759
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 3.806565564285279e-4
allele num: 65676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14494
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.163e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e-1

DP
type: SiteQuality
SIO_000300: 1.781386e6

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

QD
type: SiteQuality
SIO_000300: 1.504e1

GenotypeQuality
all individuals: 6727
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2936
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4426
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2621
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1537
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2927
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2700
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2593
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13818
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14494
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.790483649892304e-5
allele num: 10214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.522626225714112e-4
allele num: 65676
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.163e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.504e1

DP
type: SiteQuality
SIO_000300: 1.781386e6

GenotypeQuality
all individuals: 10125
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11417
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2741
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3750
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2874
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2681
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4408
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2698
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2853
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1771
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6398
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525832341542311e-5
allele num: 65538
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.807e0

MQRankSum
type: SiteQuality
SIO_000300: -4.658e0

FS
type: SiteQuality
SIO_000300: 5.083e0

MQ
type: SiteQuality
SIO_000300: 5.369e1

VQSLOD
type: SiteQuality
SIO_000300: -5.134e0

DP
type: SiteQuality
SIO_000300: 1.772544e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

QD
type: SiteQuality
SIO_000300: 6.64e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.508e0

GenotypeQuality
all individuals: 10125
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.525785779676533e-5
allele num: 65540
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South Asian
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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QD
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ReadPosRankSum
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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FS
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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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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GenotypeQuality
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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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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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African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.534730961662421e-5
allele num: 65158
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: -2.073e0

VQSLOD
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MQ
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ClippingRankSum
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MQRankSum
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FS
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QD
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InbreedingCoeff
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DP
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BaseQRankSum
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SIO_000300: -2.127e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64658
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele count: 8
allele frequency: 6.265664160401002e-4
allele num: 12768
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

DP
type: SiteQuality
SIO_000300: 2.027902e6

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.531e0

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

QD
type: SiteQuality
SIO_000300: 1.379e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 1.562744178777934e-4
allele num: 12798
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
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ClippingRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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SIO_000300: 9.0e-4

VQSLOD
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MQ
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ReadPosRankSum
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FS
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MQRankSum
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele num: 9942
num of homozygotes: 0

East Asian
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South Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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allele num: 64738
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Latino
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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QD
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MQ
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele num: 6608
num of homozygotes: 0

African
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East Asian
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Other
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Latino
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South Asian
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European (Non-Finnish)
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DP
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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Latino
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European (Non-Finnish)
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African
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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DP
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.58e-1

GenotypeQuality
all individuals: 372
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2313
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 5199
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2603
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4179
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3663
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13583
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4091
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.094222e6

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

VQSLOD
type: SiteQuality
SIO_000300: -1.069e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

QD
type: SiteQuality
SIO_000300: 1.351e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

GenotypeQuality
all individuals: 345
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13816
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20596
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4094
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5200
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4176
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3663
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.918666931164451e-5
allele num: 10082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.716e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 2.097085e6

MQ
type: SiteQuality
SIO_000300: 5.9e1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

GenotypeQuality
all individuals: 4144
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5106
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13586
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2217
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4066
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3654
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 255
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.259001161440186e-5
allele num: 13776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 28
allele frequency: 4.283572499464553e-4
allele num: 65366
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.39e-1

QD
type: SiteQuality
SIO_000300: 9.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-1

DP
type: SiteQuality
SIO_000300: 2.117229e6

FS
type: SiteQuality
SIO_000300: 2.137e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

GenotypeQuality
all individuals: 13586
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4144
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3654
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2571
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4066
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2217
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20603
bin: 9.75e1
variant carriers: 8

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13776
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10092
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.946856547412296e-4
allele num: 11516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.059694642474681e-5
allele num: 65366
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

FS
type: SiteQuality
SIO_000300: 2.137e0

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

DP
type: SiteQuality
SIO_000300: 2.117229e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-1

QD
type: SiteQuality
SIO_000300: 9.24e0

GenotypeQuality
all individuals: 145
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 436
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20631
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3685
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2612
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5231
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1740
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4211
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2242
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14037
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.157943492357573e-3
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.526093088857546e-4
allele num: 14180
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.384e0

FS
type: SiteQuality
SIO_000300: 1.378e0

MQRankSum
type: SiteQuality
SIO_000300: -2.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.917e0

VQSLOD
type: SiteQuality
SIO_000300: 7.97e-1

DP
type: SiteQuality
SIO_000300: 2.119807e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeQuality
all individuals: 155
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20662
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3694
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5437
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16124
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4255
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4128
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.054690329590728e-5
allele num: 66264
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.301e0

QD
type: SiteQuality
SIO_000300: 3.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.19e0

MQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

DP
type: SiteQuality
SIO_000300: 2.143482e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.4924e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.164e0

GenotypeDepth
all individuals: 10139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4259
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5487
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3696
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16660
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2668
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20672
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504573904670197e-5
allele num: 66464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15942
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.409e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 2.150639e6

FS
type: SiteQuality
SIO_000300: 1.4166e1

QD
type: SiteQuality
SIO_000300: 1.202e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.16e-1

GenotypeDepth
all individuals: 663
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16660
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4259
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3696
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2668
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5487
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20672
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15942
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: 8652
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 1.11e-2

ReadPosRankSum
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FS
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SIO_000300: 1.4166e1

ClippingRankSum
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SIO_000300: 1.48e0

MQ
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SIO_000300: 5.969e1

BaseQRankSum
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SIO_000300: -4.16e-1

MQRankSum
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SIO_000300: 1.8e0

VQSLOD
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SIO_000300: -2.409e0

DP
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SIO_000300: 2.150639e6

QD
type: SiteQuality
SIO_000300: 1.202e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
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allele count: 3
allele frequency: 3.467406380027739e-4
allele num: 8652
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16218
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.008712633318311e-5
allele num: 66570
num of homozygotes: 0

DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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SIO_000300: 5.52e-1

MQRankSum
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QD
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InbreedingCoeff
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SIO_000300: 3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQ
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SIO_000300: 5.93e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQ
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BaseQRankSum
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SIO_000300: 5.2e-2

FS
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SIO_000300: 1.958e0

InbreedingCoeff
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SIO_000300: 1.66e-2

MQRankSum
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QD
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SIO_000300: 9.48e0

ClippingRankSum
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SIO_000300: -1.661e0

DP
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SIO_000300: 2.157363e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.342e0

ClippingRankSum
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QD
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MQRankSum
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SIO_000300: 1.3e0

ReadPosRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

DP
type: SiteQuality
SIO_000300: 2.159817e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

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

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

Latino
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allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
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MQRankSum
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FS
type: SiteQuality
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ClippingRankSum
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DP
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MQ
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
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allele num: 908
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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East Asian
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DP
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MQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

European (Non-Finnish)
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allele count: 13
allele frequency: 1.948499655265446e-4
allele num: 66718
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South Asian
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 1.814333232537043e-3
allele num: 6614
num of homozygotes: 0

African
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Other
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QD
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DP
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

Other
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

Latino
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East Asian
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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VQSLOD
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20670
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.314e1

DP
type: SiteQuality
SIO_000300: 2.163256e6

FS
type: SiteQuality
SIO_000300: 1.7328e1

VQSLOD
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SIO_000300: -2.372e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.071e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 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: 8652
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.585e0

DP
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SIO_000300: 2.16324e6

FS
type: SiteQuality
SIO_000300: 7.376e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.007e0

QD
type: SiteQuality
SIO_000300: 1.397e1

VQSLOD
type: SiteQuality
SIO_000300: 5.570000000000001e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

DP
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SIO_000300: 2.16338e6

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.51e0

MQRankSum
type: SiteQuality
SIO_000300: 2.1e0

VQSLOD
type: SiteQuality
SIO_000300: -8.937e-1

FS
type: SiteQuality
SIO_000300: 3.426e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e0

QD
type: SiteQuality
SIO_000300: 1.441e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.465e0

MQRankSum
type: SiteQuality
SIO_000300: -6.16e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.2013e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-3

DP
type: SiteQuality
SIO_000300: 2.163281e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.66e0

QD
type: SiteQuality
SIO_000300: 1.22e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 8.029999999999999e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.946e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

DP
type: SiteQuality
SIO_000300: 2.163168e6

FS
type: SiteQuality
SIO_000300: 2.016e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.395e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: -1.012e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.33e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.7e0

MQRankSum
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SIO_000300: -1.021e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.56e-2

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.83e-1

MQ
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SIO_000300: 5.952e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

QD
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SIO_000300: 1.215e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

South Asian
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allele count: 0
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East Asian
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.924e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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DP
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SIO_000300: 2.163026e6

FS
type: SiteQuality
SIO_000300: 2.089e0

ClippingRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -9.69e-1

InbreedingCoeff
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.161728e6

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

FS
type: SiteQuality
SIO_000300: 2.388e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
all individuals: 16735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20679
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2682
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3701
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4271
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.503017021404341e-5
allele num: 66622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.749999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

FS
type: SiteQuality
SIO_000300: 8.128e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.052e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 2.158746e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.47e-1

QD
type: SiteQuality
SIO_000300: 1.375e1

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2668
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4123
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20681
bin: 9.75e1
variant carriers: 18

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3695
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 18
allele frequency: 1.736111111111111e-3
allele num: 10368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16202
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 2.158142e6

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

FS
type: SiteQuality
SIO_000300: 5.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

QD
type: SiteQuality
SIO_000300: 1.507e1

GenotypeQuality
all individuals: 435
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3694
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2634
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4227
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5283
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4118
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14269
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20680
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66344
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

FS
type: SiteQuality
SIO_000300: 7.66e-1

DP
type: SiteQuality
SIO_000300: 2.128724e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

QD
type: SiteQuality
SIO_000300: 1.303e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.22e0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14269
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2634
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4227
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4118
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2023
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3694
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20680
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15406
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.593809441466367e-4
allele num: 11566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.271020727414939e-3
allele num: 10228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.205836247437598e-4
allele num: 66344
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.303e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

VQSLOD
type: SiteQuality
SIO_000300: 4.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

FS
type: SiteQuality
SIO_000300: 7.66e-1

DP
type: SiteQuality
SIO_000300: 2.128724e6

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2098
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 452
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variant carriers: 0

GenotypeQuality
all individuals: 2629
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 4116
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variant carriers: 0

GenotypeQuality
all individuals: 5293
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4227
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3695
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20676
bin: 9.75e1
variant carriers: 9

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.495193556767992e-4
allele num: 15396
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.21e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-2

FS
type: SiteQuality
SIO_000300: 3.02e0

VQSLOD
type: SiteQuality
SIO_000300: 2.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

QD
type: SiteQuality
SIO_000300: 1.602e1

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

DP
type: SiteQuality
SIO_000300: 2.125884e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3695
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4118
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13798
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variant carriers: 0

GenotypeQuality
all individuals: 93
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GenotypeQuality
all individuals: 2301
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 230
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variant carriers: 0

GenotypeQuality
all individuals: 5278
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variant carriers: 0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
all individuals: 2630
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variant carriers: 0

GenotypeQuality
all individuals: 523
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 574
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variant carriers: 0

GenotypeQuality
all individuals: 4224
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2256
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66278
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 4.461e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.874e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.526e0

DP
type: SiteQuality
SIO_000300: 2.119786e6

VQSLOD
type: SiteQuality
SIO_000300: 8.52e-1

QD
type: SiteQuality
SIO_000300: 1.165e1

GenotypeQuality
all individuals: 20666
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12471
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 764
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variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 179
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GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5200
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4115
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3695
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 2620
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2724
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2255
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511670093118878e-5
allele num: 66152
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14992
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.23e-1

QD
type: SiteQuality
SIO_000300: 1.695e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQ
type: SiteQuality
SIO_000300: 5.997e1

DP
type: SiteQuality
SIO_000300: 2.104041e6

GenotypeQuality
all individuals: 188
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2788
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4115
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20669
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2616
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 5163
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 120
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11713
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3696
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.025993282294913e-5
allele num: 66094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14916
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.973e0

DP
type: SiteQuality
SIO_000300: 2.097269e6

QD
type: SiteQuality
SIO_000300: 1.422e1

MQRankSum
type: SiteQuality
SIO_000300: -3.99e-1

FS
type: SiteQuality
SIO_000300: 9.44e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 8.88e-1

GenotypeQuality
all individuals: 20669
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11713
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512996641147457e-5
allele num: 66094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14916
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.192107995846313e-4
allele num: 11556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.973e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 1.422e1

DP
type: SiteQuality
SIO_000300: 2.097269e6

VQSLOD
type: SiteQuality
SIO_000300: 8.88e-1

FS
type: SiteQuality
SIO_000300: 9.44e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -3.99e-1

GenotypeQuality
all individuals: 2254
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.72314105149926e-4
allele num: 14874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.428e0

DP
type: SiteQuality
SIO_000300: 2.097129e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

QD
type: SiteQuality
SIO_000300: 1.266e1

GenotypeQuality
all individuals: 1362
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 314
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variant carriers: 0

GenotypeQuality
all individuals: 2471
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518787400139728e-5
allele num: 65842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.35e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.124e0

VQSLOD
type: SiteQuality
SIO_000300: 3.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.547e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

DP
type: SiteQuality
SIO_000300: 2.085691e6

QD
type: SiteQuality
SIO_000300: 1.124e1

GenotypeQuality
all individuals: 1355
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1032
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 399
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GenotypeQuality
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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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
all individuals: 10267
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.041085059149104e-5
allele num: 65766
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9980
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e-2

DP
type: SiteQuality
SIO_000300: 2.083311e6

MQRankSum
type: SiteQuality
SIO_000300: 6.879999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 2.088e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.899e0

QD
type: SiteQuality
SIO_000300: 1.396e1

GenotypeQuality
all individuals: 486
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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GenotypeQuality
all individuals: 1251
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9606
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.57952930026852e-4
allele num: 12662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.746118e6

VQSLOD
type: SiteQuality
SIO_000300: 5.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

MQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.88e-1

QD
type: SiteQuality
SIO_000300: 1.344e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554678026180778e-5
allele num: 64322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.198e1

DP
type: SiteQuality
SIO_000300: 1.751199e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64452
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.039068994181214e-4
allele num: 9624
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.81372089388967e-5
allele num: 12798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.738203425375742e-5
allele num: 11444
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 2.398e0

QD
type: SiteQuality
SIO_000300: 1.529e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

MQ
type: SiteQuality
SIO_000300: 5.857e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

DP
type: SiteQuality
SIO_000300: 1.779418e6

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
all individuals: 5755
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variant carriers: 0

GenotypeQuality
all individuals: 3029
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55077228459773e-5
allele num: 64484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.781687e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

VQSLOD
type: SiteQuality
SIO_000300: -3.057e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.75e0

MQRankSum
type: SiteQuality
SIO_000300: -1.787e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

MQ
type: SiteQuality
SIO_000300: 5.886e1

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

GenotypeQuality
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3165
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14001
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4380
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3086
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5929
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4654
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 224
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3191
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64610
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169590643274854e-4
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9662
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-2

DP
type: SiteQuality
SIO_000300: 1.801246e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

VQSLOD
type: SiteQuality
SIO_000300: -2.926e0

QD
type: SiteQuality
SIO_000300: 9.3e-1

FS
type: SiteQuality
SIO_000300: 4.674e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

GenotypeQuality
all individuals: 215
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 267
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
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GenotypeQuality
all individuals: 1326
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2238
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4671
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5972
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.62660158633313e-5
allele num: 13112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.546503355912282e-5
allele num: 64662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.369e1

DP
type: SiteQuality
SIO_000300: 1.806555e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e0

GenotypeQuality
all individuals: 1159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2253
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6052
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variant carriers: 1

GenotypeQuality
all individuals: 231
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3129
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 4424
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4697
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14177
bin: 9.75e1
variant carriers: 186

GenotypeQuality
all individuals: 251
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.615974886641088e-4
allele num: 11468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.080814007349535e-4
allele num: 64766
num of homozygotes: 0

South Asian
type: Population
allele count: 177
allele frequency: 1.332229414421195e-2
allele num: 13286
num of homozygotes: 2

Other
type: Population
allele count: 1
allele frequency: 1.15473441108545e-3
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.031353135313531e-4
allele num: 9696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.01e-1

DP
type: SiteQuality
SIO_000300: 1.816753e6

VQSLOD
type: SiteQuality
SIO_000300: 4.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

QD
type: SiteQuality
SIO_000300: 1.334e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

GenotypeQuality
all individuals: 3209
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2252
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 73
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 234
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4682
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1005
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 579
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3125
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2887
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 199
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 15889
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 215
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14552
bin: 9.75e1
variant carriers: 682

GenotypeQuality
all individuals: 195
bin: 7.5e0
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 7.481669908723627e-5
allele num: 13366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.232893601282209e-4
allele num: 64888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Latino
type: Population
allele count: 35
allele frequency: 3.051438535309503e-3
allele num: 11470
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.149425287356322e-3
allele num: 870
num of homozygotes: 0

African
type: Population
allele count: 669
allele frequency: 6.862946245383668e-2
allele num: 9748
num of homozygotes: 20

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.28e1

DP
type: SiteQuality
SIO_000300: 1.835285e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.116e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

FS
type: SiteQuality
SIO_000300: 1.348e0

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.94e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.87e0

GenotypeQuality
all individuals: 732
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4750
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2854
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
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variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14225
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4476
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variant carriers: 0

GenotypeQuality
all individuals: 178
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variant carriers: 0

GenotypeQuality
all individuals: 196
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variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3170
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.238444245988976e-5
allele num: 64946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.48e-1

FS
type: SiteQuality
SIO_000300: 1.293e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e0

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

DP
type: SiteQuality
SIO_000300: 1.836009e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

QD
type: SiteQuality
SIO_000300: 1.113e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.91e-1

GenotypeQuality
all individuals: 205
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
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variant carriers: 0

GenotypeQuality
all individuals: 169
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variant carriers: 0

GenotypeQuality
all individuals: 3165
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2285
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variant carriers: 0

GenotypeQuality
all individuals: 2811
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 4478
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variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
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variant carriers: 0

GenotypeQuality
all individuals: 3252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6120
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14223
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64976
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13560
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.214e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

DP
type: SiteQuality
SIO_000300: 1.838016e6

VQSLOD
type: SiteQuality
SIO_000300: -6.217e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.7e-1

MQ
type: SiteQuality
SIO_000300: 5.742e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.54e0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16442
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3248
bin: 9.25e1
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GenotypeQuality
all individuals: 14231
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2767
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4762
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4486
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65022
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 6.622516556291391e-4
allele num: 13590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.839931e6

QD
type: SiteQuality
SIO_000300: 1.429e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e-1

GenotypeQuality
all individuals: 3310
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2343
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 113
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19810
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4613
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6594
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14284
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4968
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3368
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 4.524068041983351e-5
allele num: 66312
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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DP
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MQ
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ClippingRankSum
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QD
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InbreedingCoeff
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SIO_000300: 3.0e-4

MQRankSum
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 1.74e-1

VQSLOD
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FS
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SIO_000300: 1.412e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66470
num of homozygotes: 0

Other
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African
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allele frequency: 0.0e0
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South Asian
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allele num: 16352
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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BaseQRankSum
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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ClippingRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.503714174009804e-5
allele num: 66502
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1

African
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allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503849855630414e-5
allele num: 66496
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
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SIO_000300: 2.16e-1

BaseQRankSum
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SIO_000300: 4.22e0

MQRankSum
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QD
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MQ
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 1.143e0

ReadPosRankSum
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DP
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SIO_000300: 1.91572e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.503171692270691e-5
allele num: 66526
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Other
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MQ
type: SiteQuality
SIO_000300: 5.984e1

ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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QD
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DP
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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South Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 5.78168362627197e-4
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FS
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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South Asian
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East Asian
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ReadPosRankSum
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MQRankSum
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DP
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QD
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VQSLOD
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FS
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MQ
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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African
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East Asian
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Other
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European (Non-Finnish)
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allele num: 66536
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Latino
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QD
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InbreedingCoeff
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ReadPosRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3399
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5016
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4659
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14309
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 288
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2349
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.734003814808393e-4
allele num: 11534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.334e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.35e0

VQSLOD
type: SiteQuality
SIO_000300: -3.889e-1

DP
type: SiteQuality
SIO_000300: 1.919944e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 9.869999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-2