1-212968511-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212968511
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212968511
    reference: chr 1
allele count: 8
allele frequency: 6.610586854848039e-5
allele num: 121018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.99+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.92+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.95+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.99+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.99+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.96+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.100+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.99+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.99+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.99+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.258+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.99+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.99+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.97+42A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.143+42A>T
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

1-212968513-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212968513
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212968513
    reference: chr 1
allele count: 1
allele frequency: 8.269793751343841e-6
allele num: 120922
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.92+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.99+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.99+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.100+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.99+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.96+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.95+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.97+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.99+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.99+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.99+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.143+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.99+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.258+44C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.99+44C>T
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8798
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-212968517-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212968517
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212968517
    reference: chr 1
allele count: 2
allele frequency: 1.655985559805918e-5
allele num: 120774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.99+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.99+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.99+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.99+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.95+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.99+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.258+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.143+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.99+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.97+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.99+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.99+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.92+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.96+48C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.100+48C>A
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9986
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

1-212969818-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969818
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969818
    reference: chr 1
allele count: 1
allele frequency: 2.511931675458427e-5
allele num: 39810
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.101-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.100-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.100-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.100-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.259-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.100-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.100-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.100-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.144-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.96-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.98-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.100-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.100-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.97-41A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.93-41A>G
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

1-212969820-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969820
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969820
    reference: chr 1
allele count: 1
allele frequency: 2.46669955599408e-5
allele num: 40540
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.96-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.100-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.100-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.144-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.98-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.100-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.100-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.100-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.101-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.93-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.97-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.100-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.100-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.100-39G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.259-39G>A
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25173
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

1-212969826-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969826
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969826
    reference: chr 1
allele count: 1
allele frequency: 2.12965329244399e-5
allele num: 46956
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.100-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.259-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.144-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.100-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.100-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.93-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.100-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.100-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.96-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.97-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.98-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.100-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.100-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.101-33T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.100-33T>C
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9632
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-212969829-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969829
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969829
    reference: chr 1
allele count: 2
allele frequency: 3.872516748634938e-5
allele num: 51646
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.98-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.97-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.100-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.96-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.100-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.259-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.144-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.100-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.100-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.100-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.100-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.93-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.100-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.101-30T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.100-30T>G
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-212969831-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969831
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969831
    reference: chr 1
allele count: 8
allele frequency: 1.496949964447438e-4
allele num: 53442
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.100-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.96-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.100-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.101-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.259-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.100-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.98-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.100-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.100-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.144-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.100-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.100-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.93-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.100-28G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.97-28G>A
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23724
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-212969838-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969838
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969838
    reference: chr 1
allele count: 1
allele frequency: 1.566170712607674e-5
allele num: 63850
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.100-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.100-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.144-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.97-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.100-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.259-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.100-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.98-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.96-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.100-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.100-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.100-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.100-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.101-21T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.93-21T>C
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4628
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

1-212969842-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969842
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969843
    reference: chr 1
allele count: 34801
allele frequency: 4.027613823114136e-1
allele num: 86406
alternate allele: CT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.100-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.100-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.100-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.259-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.144-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.100-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.100-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.100-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.93-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.100-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.97-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.101-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.96-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.98-4dupT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.100-4dupT
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 7.5e0
  variant carriers: 2767
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 184
genotype depth: GenotypeDepth
  all individuals: 7014
  bin: 2.75e1
  variant carriers: 4741
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 3.25e1
  variant carriers: 2649
genotype depth: GenotypeDepth
  all individuals: 11464
  bin: 2.25e1
  variant carriers: 7892
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.25e1
  variant carriers: 453
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 282
genotype depth: GenotypeDepth
  all individuals: 11244
  bin: 1.25e1
  variant carriers: 8180
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 130
genotype quality: GenotypeQuality
num of homozygotes: 610
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

1-212969842-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969842
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969841
    reference: chr 1
allele count: 9188
allele frequency: 1.06335208203134e-1
allele num: 86406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.93-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.100-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.100-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.100-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.100-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.101-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.97-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.259-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.100-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.100-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.100-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.98-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.96-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.144-4delT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.100-4delT
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7014
  bin: 2.75e1
  variant carriers: 1744
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 3.75e1
  variant carriers: 541
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 1.75e1
  variant carriers: 2478
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 4.25e1
  variant carriers: 398
genotype depth: GenotypeDepth
  all individuals: 11244
  bin: 1.25e1
  variant carriers: 1324
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 37
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: CT
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

1-212969842-C-CTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969842
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969844
    reference: chr 1
allele count: 959
allele frequency: 1.109876628937805e-2
allele num: 86406
alternate allele: CTT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.100-5_100-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.100-5_100-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.100-5_100-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.97-5_97-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.100-5_100-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.98-5_98-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.100-5_100-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.100-5_100-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.259-5_259-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.100-5_100-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.93-5_93-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.96-5_96-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.101-5_101-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.144-5_144-4dupTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.100-5_100-4dupTT
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11244
  bin: 1.25e1
  variant carriers: 365
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 1.75e1
  variant carriers: 416
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 7.5e0
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 11464
  bin: 2.25e1
  variant carriers: 286
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 3.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

1-212969842-C-CTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969842
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969845
    reference: chr 1
allele count: 23
allele frequency: 2.661852186190774e-4
allele num: 86406
alternate allele: CTTT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.100-6_100-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.259-6_259-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.98-6_98-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.100-6_100-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.96-6_96-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.100-6_100-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.100-6_100-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.100-6_100-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.144-6_144-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.100-6_100-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.97-6_97-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.93-6_93-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.101-6_101-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.100-6_100-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.100-6_100-4dupTTT
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11244
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7014
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

1-212969842-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969842
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969840
    reference: chr 1
allele count: 330
allele frequency: 3.819179223665023e-3
allele num: 86406
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.100-5_100-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.96-5_96-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.100-5_100-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.100-5_100-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.100-5_100-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.259-5_259-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.100-5_100-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.93-5_93-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.98-5_98-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.100-5_100-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.97-5_97-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.100-5_100-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.144-5_144-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.101-5_101-4delTT
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.100-5_100-4delTT
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 7014
  bin: 2.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11244
  bin: 1.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 3.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 11464
  bin: 2.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: CTT
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

1-212969842-CTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969842
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969839
    reference: chr 1
allele count: 11
allele frequency: 1.273059741221675e-4
allele num: 86406
alternate allele: C
canonical: false
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11244
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7014
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11464
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1429
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1968
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2073
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2244
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2285
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8124
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18581
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1425
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1838
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 1.440092165898618e-4
  allele num: 6944
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 3
  allele frequency: 3.646973012399708e-4
  allele num: 8226
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5884
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 2
  allele frequency: 3.810975609756098e-4
  allele num: 5248
  num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: CTTT
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

1-212969863-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969863
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969863
    reference: chr 1
allele count: 16
allele frequency: 1.341314152540952e-4
allele num: 119286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.101A>G
  hgvsp: ENSP00000434276.2:p.Asn34Ser
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.97A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.104A>G
  hgvsp: ENSP00000355941.4:p.Asn35Ser
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.104A>G
  hgvsp: ENSP00000434428.1:p.Asn35Ser
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.102A>G
  hgvsp: ENSP00000431379.1:p.Asn35Ser
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.148A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.100A>G
  hgvsp: ENSP00000433143.1:p.Asn34Ser
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.105A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.263A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.104A>G
  hgvsp: ENSP00000431376.1:p.Asn35Ser
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.104A>G
  hgvsp: ENSP00000355940.4:p.Asn35Ser
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.104A>G
  hgvsp: ENSP00000432730.1:p.Asn35Ser
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.104A>G
  hgvsp: ENSP00000436364.1:p.Asn35Ser
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.104A>G
  hgvsp: ENSP00000434801.1:p.Asn35Ser
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.104A>G
  hgvsp: ENSP00000433755.1:p.Asn35Ser
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20428
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3634
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn35Ser
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

1-212969867-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969867
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969867
    reference: chr 1
allele count: 1
allele frequency: 8.359246999030327e-6
allele num: 119628
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.267T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.108T>C
  hgvsp: ENST00000532324.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.108T>C
  hgvsp: ENST00000526641.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.108T>C
  hgvsp: ENST00000366973.4:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.105T>C
  hgvsp: ENST00000530399.2:c.105T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.108T>C
  hgvsp: ENST00000366974.4:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.101T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.109T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.108T>C
  hgvsp: ENST00000530441.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.108T>C
  hgvsp: ENST00000531963.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.106T>C
  hgvsp: ENST00000488246.2:c.106T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.108T>C
  hgvsp: ENST00000533650.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.104T>C
  hgvsp: ENST00000525574.1:c.104T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.152T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.108T>C
  hgvsp: ENST00000526997.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val36Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-212969871-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969871
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969871
    reference: chr 1
allele count: 1
allele frequency: 8.343623802689983e-6
allele num: 119852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.156G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.112G>C
  hgvsp: ENSP00000355940.4:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.109G>C
  hgvsp: ENSP00000434276.2:p.Ala37Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.112G>C
  hgvsp: ENSP00000436364.1:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.110G>C
  hgvsp: ENSP00000431379.1:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.271G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.112G>C
  hgvsp: ENSP00000432730.1:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.108G>C
  hgvsp: ENSP00000433143.1:p.Ala37Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.113G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.112G>C
  hgvsp: ENSP00000434801.1:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.112G>C
  hgvsp: ENSP00000355941.4:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.112G>C
  hgvsp: ENSP00000433755.1:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.105G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.112G>C
  hgvsp: ENSP00000431376.1:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.112G>C
  hgvsp: ENSP00000434428.1:p.Ala38Pro
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala38Pro
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ

1-212969871-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969871
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969870
    reference: chr 1
allele count: 1
allele frequency: 8.343623802689983e-6
allele num: 119852
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.274delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.108delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.115delC
  hgvsp: ENSP00000433755.1:p.Val40TrpfsTer46
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.113delC
  hgvsp: ENSP00000431379.1:p.Val40TrpfsTer46
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.115delC
  hgvsp: ENSP00000434428.1:p.Val40TrpfsTer46
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.115delC
  hgvsp: ENSP00000355940.4:p.Val40TrpfsTer46
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.115delC
  hgvsp: ENSP00000432730.1:p.Val40TrpfsTer28
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.116delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.115delC
  hgvsp: ENSP00000436364.1:p.Val40TrpfsTer46
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.115delC
  hgvsp: ENSP00000355941.4:p.Val40TrpfsTer46
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.112delC
  hgvsp: ENSP00000434276.2:p.Val39TrpfsTer46
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.111delC
  hgvsp: ENSP00000433143.1:p.Val39TrpfsTer28
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.115delC
  hgvsp: ENSP00000431376.1:p.Val40TrpfsTer46
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.159delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.115delC
  hgvsp: ENSP00000434801.1:p.Val40TrpfsTer46
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val40TrpfsTer46
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: GC
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

1-212969873-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969873
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969873
    reference: chr 1
allele count: 1
allele frequency: 8.334722453742291e-6
allele num: 119980
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.112C>G
  hgvsp: ENST00000488246.2:c.112C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.158C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.110C>G
  hgvsp: ENST00000525574.1:c.110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.114C>G
  hgvsp: ENST00000526641.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.115C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.114C>G
  hgvsp: ENST00000530441.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.107C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.114C>G
  hgvsp: ENST00000533650.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.114C>G
  hgvsp: ENST00000366973.4:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.114C>G
  hgvsp: ENST00000366974.4:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.273C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.111C>G
  hgvsp: ENST00000530399.2:c.111C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.114C>G
  hgvsp: ENST00000531963.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.114C>G
  hgvsp: ENST00000526997.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.114C>G
  hgvsp: ENST00000532324.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20952
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala38Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

1-212969884-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969884
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969884
    reference: chr 1
allele count: 78
allele frequency: 6.541209620609842e-4
allele num: 119244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.169T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.125T>G
  hgvsp: ENSP00000355941.4:p.Val42Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.125T>G
  hgvsp: ENSP00000434428.1:p.Val42Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.284T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.121T>G
  hgvsp: ENSP00000433143.1:p.Val41Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.126T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.122T>G
  hgvsp: ENSP00000434276.2:p.Val41Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.118T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.125T>G
  hgvsp: ENSP00000432730.1:p.Val42Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.125T>G
  hgvsp: ENSP00000355940.4:p.Val42Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.125T>G
  hgvsp: ENSP00000431376.1:p.Val42Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.125T>G
  hgvsp: ENSP00000434801.1:p.Val42Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.125T>G
  hgvsp: ENSP00000433755.1:p.Val42Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.123T>G
  hgvsp: ENSP00000431379.1:p.Val42Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.125T>G
  hgvsp: ENSP00000436364.1:p.Val42Gly
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 19192
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val42Gly
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

1-212969888-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969888
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969888
    reference: chr 1
allele count: 8
allele frequency: 6.651700340899642e-5
allele num: 120270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.129C>T
  hgvsp: ENST00000366973.4:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.130C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.126C>T
  hgvsp: ENST00000530399.2:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.129C>T
  hgvsp: ENST00000530441.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.129C>T
  hgvsp: ENST00000366974.4:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.127C>T
  hgvsp: ENST00000488246.2:c.127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.288C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.129C>T
  hgvsp: ENST00000531963.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.122C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.129C>T
  hgvsp: ENST00000532324.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.125C>T
  hgvsp: ENST00000525574.1:c.125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.129C>T
  hgvsp: ENST00000526997.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.129C>T
  hgvsp: ENST00000526641.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.129C>T
  hgvsp: ENST00000533650.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.173C>T
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala43Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

1-212969889-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969889
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969889
    reference: chr 1
allele count: 98
allele frequency: 8.146165483533109e-4
allele num: 120302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.131G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.130G>A
  hgvsp: ENSP00000355940.4:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.289G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.127G>A
  hgvsp: ENSP00000434276.2:p.Glu43Lys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.126G>A
  hgvsp: ENSP00000433143.1:p.Glu43Lys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.130G>A
  hgvsp: ENSP00000433755.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.128G>A
  hgvsp: ENSP00000431379.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.130G>A
  hgvsp: ENSP00000436364.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.123G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.130G>A
  hgvsp: ENSP00000355941.4:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.130G>A
  hgvsp: ENSP00000432730.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.174G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.130G>A
  hgvsp: ENSP00000434428.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.130G>A
  hgvsp: ENSP00000434801.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.130G>A
  hgvsp: ENSP00000431376.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 21080
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu44Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-212969892-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969892
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969892
    reference: chr 1
allele count: 1
allele frequency: 8.30813199960121e-6
allele num: 120364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.133C>A
  hgvsp: ENSP00000434428.1:p.His45Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.130C>A
  hgvsp: ENSP00000434276.2:p.His44Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.133C>A
  hgvsp: ENSP00000355941.4:p.His45Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.133C>A
  hgvsp: ENSP00000431376.1:p.His45Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.133C>A
  hgvsp: ENSP00000355940.4:p.His45Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.133C>A
  hgvsp: ENSP00000434801.1:p.His45Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.133C>A
  hgvsp: ENSP00000436364.1:p.His45Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.126C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.133C>A
  hgvsp: ENSP00000433755.1:p.His45Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.133C>A
  hgvsp: ENSP00000432730.1:p.His45Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.131C>A
  hgvsp: ENSP00000431379.1:p.His45Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.129C>A
  hgvsp: ENSP00000433143.1:p.His44Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.292C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.134C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.177C>A
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His45Asn
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

1-212969893-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969893
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969893
    reference: chr 1
allele count: 1
allele frequency: 8.304406317992327e-6
allele num: 120418
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.134A>G
  hgvsp: ENSP00000434428.1:p.His45Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.134A>G
  hgvsp: ENSP00000355940.4:p.His45Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.178A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.134A>G
  hgvsp: ENSP00000433755.1:p.His45Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.134A>G
  hgvsp: ENSP00000355941.4:p.His45Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.134A>G
  hgvsp: ENSP00000431376.1:p.His45Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.130A>G
  hgvsp: ENSP00000433143.1:p.His44Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.135A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.134A>G
  hgvsp: ENSP00000436364.1:p.His45Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.132A>G
  hgvsp: ENSP00000431379.1:p.His45Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.293A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.127A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.134A>G
  hgvsp: ENSP00000432730.1:p.His45Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.131A>G
  hgvsp: ENSP00000434276.2:p.His44Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.134A>G
  hgvsp: ENSP00000434801.1:p.His45Arg
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His45Arg
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

1-212969895-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969895
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969895
    reference: chr 1
allele count: 3
allele frequency: 2.490535963339311e-5
allele num: 120456
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.136T>C
  hgvsp: ENSP00000433755.1:p.Ser46Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.136T>C
  hgvsp: ENSP00000355941.4:p.Ser46Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.136T>C
  hgvsp: ENSP00000434428.1:p.Ser46Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.132T>C
  hgvsp: ENSP00000433143.1:p.Ser45Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.136T>C
  hgvsp: ENSP00000432730.1:p.Ser46Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.134T>C
  hgvsp: ENSP00000431379.1:p.Ser46Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.133T>C
  hgvsp: ENSP00000434276.2:p.Ser45Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.136T>C
  hgvsp: ENSP00000355940.4:p.Ser46Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.136T>C
  hgvsp: ENSP00000436364.1:p.Ser46Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.295T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.137T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.180T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.136T>C
  hgvsp: ENSP00000434801.1:p.Ser46Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.136T>C
  hgvsp: ENSP00000431376.1:p.Ser46Pro
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.129T>C
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21260
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser46Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

1-212969900-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969900
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969900
    reference: chr 1
allele count: 3
allele frequency: 2.488965585902499e-5
allele num: 120532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.141A>G
  hgvsp: ENST00000530441.1:c.141A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.138A>G
  hgvsp: ENST00000530399.2:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.300A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.137A>G
  hgvsp: ENST00000525574.1:c.137A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.134A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.142A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.141A>G
  hgvsp: ENST00000526641.1:c.141A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.141A>G
  hgvsp: ENST00000526997.1:c.141A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.141A>G
  hgvsp: ENST00000531963.1:c.141A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.141A>G
  hgvsp: ENST00000532324.1:c.141A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.141A>G
  hgvsp: ENST00000366974.4:c.141A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.141A>G
  hgvsp: ENST00000533650.1:c.141A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.141A>G
  hgvsp: ENST00000366973.4:c.141A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.185A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.139A>G
  hgvsp: ENST00000488246.2:c.139A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly47Gly
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

1-212969906-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969906
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969906
    reference: chr 1
allele count: 136
allele frequency: 1.127657457464097e-3
allele num: 120604
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.147T>A
  hgvsp: ENSP00000434801.1:p.Phe49Leu
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.147T>A
  hgvsp: ENSP00000431376.1:p.Phe49Leu
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.147T>A
  hgvsp: ENSP00000355940.4:p.Phe49Leu
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.147T>A
  hgvsp: ENSP00000432730.1:p.Phe49Leu
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.147T>A
  hgvsp: ENSP00000433755.1:p.Phe49Leu
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.147T>A
  hgvsp: ENSP00000436364.1:p.Phe49Leu
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.147T>A
  hgvsp: ENSP00000434428.1:p.Phe49Leu
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.145T>A
  hgvsp: ENSP00000431379.1:p.Phe49Leu
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.191T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.143T>A
  hgvsp: ENSP00000433143.1:p.Phe48Leu
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.144T>A
  hgvsp: ENSP00000434276.2:p.Phe48Leu
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.140T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.148T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.147T>A
  hgvsp: ENSP00000355941.4:p.Phe49Leu
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.306T>A
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21363
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 3.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Phe49Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

1-212969912-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969912
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969912
    reference: chr 1
allele count: 1
allele frequency: 8.287613333112331e-6
allele num: 120662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.153G>T
  hgvsp: ENSP00000432730.1:p.Lys51Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.153G>T
  hgvsp: ENSP00000434801.1:p.Lys51Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.153G>T
  hgvsp: ENSP00000436364.1:p.Lys51Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.146G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.153G>T
  hgvsp: ENSP00000434428.1:p.Lys51Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.197G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.150G>T
  hgvsp: ENSP00000434276.2:p.Lys50Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.312G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.151G>T
  hgvsp: ENSP00000431379.1:p.Lys51Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.153G>T
  hgvsp: ENSP00000355941.4:p.Lys51Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.153G>T
  hgvsp: ENSP00000355940.4:p.Lys51Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.153G>T
  hgvsp: ENSP00000433755.1:p.Lys51Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.153G>T
  hgvsp: ENSP00000431376.1:p.Lys51Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.154G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.149G>T
  hgvsp: ENSP00000433143.1:p.Lys50Asn
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys51Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP

1-212969917-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969917
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969917
    reference: chr 1
allele count: 2
allele frequency: 1.657165583985152e-5
allele num: 120688
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.158T>G
  hgvsp: ENSP00000434428.1:p.Met53Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.155T>G
  hgvsp: ENSP00000434276.2:p.Met52Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.158T>G
  hgvsp: ENSP00000431376.1:p.Met53Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.158T>G
  hgvsp: ENSP00000433755.1:p.Met53Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.317T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.158T>G
  hgvsp: ENSP00000355940.4:p.Met53Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.158T>G
  hgvsp: ENSP00000432730.1:p.Met53Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.158T>G
  hgvsp: ENSP00000355941.4:p.Met53Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.151T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.158T>G
  hgvsp: ENSP00000434801.1:p.Met53Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.158T>G
  hgvsp: ENSP00000436364.1:p.Met53Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.202T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.154T>G
  hgvsp: ENSP00000433143.1:p.Met52Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.156T>G
  hgvsp: ENSP00000431379.1:p.Met53Arg
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.159T>G
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met53Arg
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

1-212969928-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969928
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969928
    reference: chr 1
allele count: 3
allele frequency: 2.489130795526202e-5
allele num: 120524
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.169G>C
  hgvsp: ENSP00000355941.4:p.Glu57Gln
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.169G>C
  hgvsp: ENSP00000434801.1:p.Glu57Gln
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.169G>C
  hgvsp: ENSP00000434428.1:p.Glu57Gln
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.169G>C
  hgvsp: ENSP00000431376.1:p.Glu57Gln
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.169G>C
  hgvsp: ENSP00000436364.1:p.Glu57Gln
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.169G>C
  hgvsp: ENSP00000355940.4:p.Glu57Gln
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.166G>C
  hgvsp: ENSP00000434276.2:p.Glu56Gln
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.213G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.165G>C
  hgvsp: ENSP00000433143.1:p.Glu56Gln
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.169G>C
  hgvsp: ENSP00000433755.1:p.Glu57Gln
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.169G>C
  hgvsp: ENSP00000432730.1:p.Glu57Gln
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.167G>C
  hgvsp: ENSP00000431379.1:p.Glu57Gln
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.328G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.162G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.170G>C
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu57Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

1-212969939-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969939
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969939
    reference: chr 1
allele count: 2
allele frequency: 1.66306336271412e-5
allele num: 120260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.332+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.173+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.173+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.173+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.217+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.170+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.173+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.173+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.173+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.166+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.171+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.173+7C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.181C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+7C>T
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.173+7C>T
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

1-212969943-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969943
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969943
    reference: chr 1
allele count: 1
allele frequency: 8.320436656515735e-6
allele num: 120186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.185T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.173+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.170+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.173+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.173+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.173+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.171+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.217+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.173+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.173+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.332+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.166+11T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.173+11T>A
  variant of: http://identifiers.org/hgnc/27010
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

1-212969956-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969956
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969956
    reference: chr 1
allele count: 2
allele frequency: 1.667278001934042e-5
allele num: 119956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.173+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.173+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.171+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.217+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.166+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.332+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.170+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.173+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.173+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.173+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.173+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.173+24A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.198A>G
  variant of: http://identifiers.org/hgnc/27010
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

1-212969966-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969966
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969966
    reference: chr 1
allele count: 1
allele frequency: 8.357290900581667e-6
allele num: 119656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.173+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.208T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.173+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.166+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.170+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.217+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.171+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.173+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.332+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.173+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.173+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.173+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+34T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.173+34T>C
  variant of: http://identifiers.org/hgnc/27010
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8145
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

1-212969968-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969968
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969968
    reference: chr 1
allele count: 2
allele frequency: 1.672324698563473e-5
allele num: 119594
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.166+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.173+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.173+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.210A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.332+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.173+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.173+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.173+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.171+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.173+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.170+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.217+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+36A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.173+36A>G
  variant of: http://identifiers.org/hgnc/27010
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17893
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

1-212969970-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969970
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969970
    reference: chr 1
allele count: 1
allele frequency: 8.358967500334358e-6
allele num: 119632
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.173+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.173+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.173+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.173+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.166+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.217+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.173+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.170+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.171+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.212A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.173+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.173+38A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.332+38A>G
  variant of: http://identifiers.org/hgnc/27010
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8034
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

1-212969983-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212969983
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212969983
    reference: chr 1
allele count: 1
allele frequency: 8.410428931875526e-6
allele num: 118900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.173+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.173+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000532433
  gene symbol: TATDN3
  hgvsc: ENST00000532433.1:n.225T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.170+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.173+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.173+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.171+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.173+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.173+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.217+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.332+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.173+51T>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.166+51T>A
  variant of: http://identifiers.org/hgnc/27010
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15900
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-212970412-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970412
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970412
    reference: chr 1
allele count: 2
allele frequency: 1.690245592684617e-5
allele num: 118326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+480A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-42A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-42A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-42A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-42A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-42A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-42A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-42A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+480A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-42A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-42A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-42A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-42A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-42A>C
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15442
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

1-212970412-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970412
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970412
    reference: chr 1
allele count: 1
allele frequency: 8.451227963423086e-6
allele num: 118326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-42A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-42A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-42A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-42A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-42A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-42A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-42A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+480A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-42A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-42A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+480A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-42A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-42A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-42A>G
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15442
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

1-212970422-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970422
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970421
    reference: chr 1
allele count: 41
allele frequency: 3.441733962359183e-4
allele num: 119126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+492delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-30delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-30delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-30delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-30delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-30delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-30delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-30delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-30delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-30delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+492delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-30delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-30delC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-30delC
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 16727
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: TC
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

1-212970423-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970423
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970423
    reference: chr 1
allele count: 8
allele frequency: 6.725514922236234e-5
allele num: 118950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-31C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+491C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+491C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-31C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-31C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-31C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-31C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-31C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-31C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-31C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-31C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-31C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-31C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-31C>T
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16909
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

1-212970427-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970427
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970427
    reference: chr 1
allele count: 1
allele frequency: 8.366800535475235e-6
allele num: 119520
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-27C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-27C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-27C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-27C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-27C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+495C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-27C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+495C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-27C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-27C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-27C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-27C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-27C>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-27C>G
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17518
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

1-212970433-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970433
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970433
    reference: chr 1
allele count: 1
allele frequency: 8.337085021593051e-6
allele num: 119946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-21C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-21C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-21C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-21C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-21C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-21C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+501C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-21C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-21C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-21C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-21C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-21C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+501C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-21C>T
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31093
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

1-212970435-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970435
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970435
    reference: chr 1
allele count: 1
allele frequency: 8.324038157390913e-6
allele num: 120134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-19G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-19G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-19G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-19G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-19G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-19G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+503G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+503G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-19G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-19G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-19G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-19G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-19G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-19G>C
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31327
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-212970436-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970436
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970436
    reference: chr 1
allele count: 2
allele frequency: 1.663561352142667e-5
allele num: 120224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+504T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-18T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+504T>G
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18233
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

1-212970438-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970438
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970438
    reference: chr 1
allele count: 1
allele frequency: 8.310065150910783e-6
allele num: 120336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-16G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-16G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-16G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+506G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-16G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-16G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-16G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+506G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-16G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-16G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-16G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-16G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-16G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-16G>C
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

1-212970439-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970439
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970439
    reference: chr 1
allele count: 2862
allele frequency: 2.376326408608579e-2
allele num: 120438
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+507G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-15G>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+507G>C
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 9.75e1
  variant carriers: 232
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.25e1
  variant carriers: 182
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 378
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 3.25e1
  variant carriers: 368
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 18221
  bin: 2.75e1
  variant carriers: 308
genotype quality: GenotypeQuality
num of homozygotes: 52
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

1-212970439-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970439
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970439
    reference: chr 1
allele count: 1
allele frequency: 8.303027283747654e-6
allele num: 120438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+507G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-15G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-15G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-15G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-15G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-15G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-15G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-15G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-15G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-15G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-15G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+507G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-15G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-15G>T
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

1-212970441-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970441
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970441
    reference: chr 1
allele count: 1
allele frequency: 8.294487483618387e-6
allele num: 120562
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-13T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-13T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-13T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+509T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-13T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-13T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-13T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+509T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-13T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-13T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-13T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-13T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-13T>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-13T>C
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

1-212970446-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970446
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970446
    reference: chr 1
allele count: 2
allele frequency: 1.656506758547575e-5
allele num: 120736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+514A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-8A>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+514A>T
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.174-8A>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/1-212970446-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970446
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970446
    reference: chr 1
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+514A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-8A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-8A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-8A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+514A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-8A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-8A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-8A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-8A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-8A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-8A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-8A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-8A>C
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-8A>C
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.174-8A>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

1-212970448-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970448
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970448
    reference: chr 1
allele count: 7
allele frequency: 5.794318257069068e-5
allele num: 120808
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174-6T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167-6T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172-6T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174-6T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218-6T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171-6T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174-6T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174-6T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+516T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174-6T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174-6T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+516T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174-6T>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333-6T>G
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.174-6T>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

1-212970454-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970454
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970454
    reference: chr 1
allele count: 2
allele frequency: 1.653685237551884e-5
allele num: 120942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.174G>A
  hgvsp: ENST00000366974.4:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.174G>A
  hgvsp: ENST00000526641.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.218G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+522G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.174G>A
  hgvsp: ENST00000532324.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.174G>A
  hgvsp: ENST00000531963.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.174G>A
  hgvsp: ENST00000526997.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.171G>A
  hgvsp: ENST00000530399.2:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.174G>A
  hgvsp: ENST00000366973.4:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.333G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.174G>A
  hgvsp: ENST00000533650.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.172G>A
  hgvsp: ENST00000488246.2:c.172G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.167G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+522G>A
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.174G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

1-212970456-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970456
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970456
    reference: chr 1
allele count: 1
allele frequency: 8.265145879824779e-6
allele num: 120990
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.220A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.176A>G
  hgvsp: ENSP00000355941.4:p.Tyr59Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.173A>G
  hgvsp: ENSP00000434276.2:p.Tyr58Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.176A>G
  hgvsp: ENSP00000433755.1:p.Tyr59Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.169A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+524A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.176A>G
  hgvsp: ENSP00000434428.1:p.Tyr59Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.176A>G
  hgvsp: ENSP00000355940.4:p.Tyr59Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.176A>G
  hgvsp: ENSP00000431376.1:p.Tyr59Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.176A>G
  hgvsp: ENSP00000436364.1:p.Tyr59Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.176A>G
  hgvsp: ENSP00000434801.1:p.Tyr59Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.174A>G
  hgvsp: ENSP00000431379.1:p.Tyr59Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.335A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+524A>G
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr59Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-212970481-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970481
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970481
    reference: chr 1
allele count: 4
allele frequency: 3.30016665841625e-5
allele num: 121206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.360G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.201G>T
  hgvsp: ENSP00000355940.4:p.Leu67Phe
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000475492
  ensembl transcript: ENST00000606486
  gene symbol: TATDN3
  hgvsc: ENST00000606486.1:c.8G>T
  hgvsp: ENSP00000475492.1:p.Leu3Phe
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.201G>T
  hgvsp: ENSP00000434428.1:p.Leu67Phe
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.201G>T
  hgvsp: ENSP00000355941.4:p.Leu67Phe
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.198G>T
  hgvsp: ENSP00000434276.2:p.Leu66Phe
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+549G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.201G>T
  hgvsp: ENSP00000434801.1:p.Leu67Phe
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.201G>T
  hgvsp: ENSP00000431376.1:p.Leu67Phe
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.245G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.199G>T
  hgvsp: ENSP00000431379.1:p.Leu67Phe
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.194G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+549G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.201G>T
  hgvsp: ENSP00000433755.1:p.Leu67Phe
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.201G>T
  hgvsp: ENSP00000436364.1:p.Leu67Phe
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu67Phe
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

1-212970482-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970482
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970482
    reference: chr 1
allele count: 9
allele frequency: 7.425252458583592e-5
allele num: 121208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.199G>T
  hgvsp: ENSP00000434276.2:p.Gly67Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.202G>T
  hgvsp: ENSP00000355940.4:p.Gly68Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.361G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+550G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.202G>T
  hgvsp: ENSP00000434428.1:p.Gly68Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000475492
  ensembl transcript: ENST00000606486
  gene symbol: TATDN3
  hgvsc: ENST00000606486.1:c.9G>T
  hgvsp: ENSP00000475492.1:p.Gly4Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.202G>T
  hgvsp: ENSP00000355941.4:p.Gly68Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.202G>T
  hgvsp: ENSP00000434801.1:p.Gly68Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.200G>T
  hgvsp: ENSP00000431379.1:p.Gly68Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.202G>T
  hgvsp: ENSP00000431376.1:p.Gly68Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.202G>T
  hgvsp: ENSP00000433755.1:p.Gly68Cys
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.195G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+550G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.246G>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.202G>T
  hgvsp: ENSP00000436364.1:p.Gly68Cys
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly68Cys
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-212970517-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970517
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970517
    reference: chr 1
allele count: 1
allele frequency: 8.266649031148734e-6
allele num: 120968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.235C>T
  hgvsp: ENST00000488246.2:c.235C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.237C>T
  hgvsp: ENST00000366974.4:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000475492
  ensembl transcript: ENST00000606486
  gene symbol: TATDN3
  hgvsc: ENST00000606486.1:c.44C>T
  hgvsp: ENST00000606486.1:c.44C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.234C>T
  hgvsp: ENST00000530399.2:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.237C>T
  hgvsp: ENST00000531963.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.237C>T
  hgvsp: ENST00000533650.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.237C>T
  hgvsp: ENST00000526641.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.281C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.237C>T
  hgvsp: ENST00000526997.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+585C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.237C>T
  hgvsp: ENST00000366973.4:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.396C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.237C>T
  hgvsp: ENST00000532324.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+585C>T
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.230C>T
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20592
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp79Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

1-212970521-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970521
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970521
    reference: chr 1
allele count: 3
allele frequency: 2.481348530214554e-5
allele num: 120902
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.241A>G
  hgvsp: ENSP00000355941.4:p.Arg81Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.241A>G
  hgvsp: ENSP00000434801.1:p.Arg81Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000475492
  ensembl transcript: ENST00000606486
  gene symbol: TATDN3
  hgvsc: ENST00000606486.1:c.48A>G
  hgvsp: ENSP00000475492.1:p.Arg17Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.241A>G
  hgvsp: ENSP00000434428.1:p.Arg81Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.234A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.241A>G
  hgvsp: ENSP00000355940.4:p.Arg81Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.241A>G
  hgvsp: ENSP00000431376.1:p.Arg81Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.239A>G
  hgvsp: ENSP00000431379.1:p.Arg81Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+589A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.400A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.238A>G
  hgvsp: ENSP00000434276.2:p.Arg80Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.285A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+589A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.241A>G
  hgvsp: ENSP00000433755.1:p.Arg81Gly
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.241A>G
  hgvsp: ENSP00000436364.1:p.Arg81Gly
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg81Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

1-212970525-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970525
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970525
    reference: chr 1
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.243G>A
  hgvsp: ENSP00000431379.1:p.Ser82Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+593G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.245G>A
  hgvsp: ENSP00000355941.4:p.Ser82Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.245G>A
  hgvsp: ENSP00000434801.1:p.Ser82Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000475492
  ensembl transcript: ENST00000606486
  gene symbol: TATDN3
  hgvsc: ENST00000606486.1:c.52G>A
  hgvsp: ENSP00000475492.1:p.Ser18Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.242G>A
  hgvsp: ENSP00000434276.2:p.Ser81Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.245G>A
  hgvsp: ENSP00000436364.1:p.Ser82Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.238G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.245G>A
  hgvsp: ENSP00000431376.1:p.Ser82Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.404G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.245G>A
  hgvsp: ENSP00000355940.4:p.Ser82Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.245G>A
  hgvsp: ENSP00000434428.1:p.Ser82Asn
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+593G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.289G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.245G>A
  hgvsp: ENSP00000433755.1:p.Ser82Asn
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser82Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

1-212970527-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970527
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970527
    reference: chr 1
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.247G>A
  hgvsp: ENSP00000355941.4:p.Val83Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.244G>A
  hgvsp: ENSP00000434276.2:p.Val82Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.247G>A
  hgvsp: ENSP00000434801.1:p.Val83Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.247G>A
  hgvsp: ENSP00000434428.1:p.Val83Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.247G>A
  hgvsp: ENSP00000433755.1:p.Val83Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.247G>A
  hgvsp: ENSP00000431376.1:p.Val83Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.291G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.247G>A
  hgvsp: ENSP00000355940.4:p.Val83Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.240G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+595G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.247G>A
  hgvsp: ENSP00000436364.1:p.Val83Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+595G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.245G>A
  hgvsp: ENSP00000431379.1:p.Val83Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.406G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000475492
  ensembl transcript: ENST00000606486
  gene symbol: TATDN3
  hgvsc: ENST00000606486.1:c.54G>A
  hgvsp: ENSP00000475492.1:p.Val19Ile
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20573
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val83Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/1-212970533-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970533
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970533
    reference: chr 1
allele count: 214
allele frequency: 1.781403479563806e-3
allele num: 120130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.253C>A
  hgvsp: ENSP00000436364.1:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.253C>A
  hgvsp: ENSP00000431376.1:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.253C>A
  hgvsp: ENSP00000434428.1:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.253C>A
  hgvsp: ENSP00000434801.1:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.253C>A
  hgvsp: ENSP00000355941.4:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.251C>A
  hgvsp: ENSP00000431379.1:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.250C>A
  hgvsp: ENSP00000434276.2:p.Leu84Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000475492
  ensembl transcript: ENST00000606486
  gene symbol: TATDN3
  hgvsc: ENST00000606486.1:c.60C>A
  hgvsp: ENSP00000475492.1:p.Leu21Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.253C>A
  hgvsp: ENSP00000355940.4:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.246C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+601C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+601C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.412C>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.253C>A
  hgvsp: ENSP00000433755.1:p.Leu85Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.297C>A
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 20500
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 3.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
hgvs: p.Leu85Ile
num of homozygotes: 2
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

1-212970539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970539
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970539
    reference: chr 1
allele count: 9
allele frequency: 7.531758916765696e-5
allele num: 119494
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.256+1G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.251+1G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.255+1G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.417+1G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.258+1G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.258+1G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.258+1G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.258+1G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000475492
  ensembl transcript: ENST00000606486
  gene symbol: TATDN3
  hgvsc: ENST00000606486.1:c.66G>A
  hgvsp: ENSP00000475492.1:p.Val23Ile
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.258+1G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.258+1G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+607G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.302+1G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+607G>A
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.258+1G>A
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20494
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28788
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.258+1G>A
num of homozygotes: 1
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

1-212970544-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970544
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970544
    reference: chr 1
allele count: 1
allele frequency: 8.451942256330504e-6
allele num: 118316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+612A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.258+6A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.256+6A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.258+6A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.258+6A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.417+6A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.302+6A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.258+6A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+612A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.255+6A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.258+6A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000475492
  ensembl transcript: ENST00000606486
  gene symbol: TATDN3
  hgvsc: ENST00000606486.1:c.71A>G
  hgvsp: ENST00000606486.1:c.71A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.258+6A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.258+6A>G
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.251+6A>G
  variant of: http://identifiers.org/hgnc/27010
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27649
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.258+6A>G
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

1-212970544-AGTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 212970544
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 212970541
    reference: chr 1
allele count: 1
allele frequency: 8.451942256330504e-6
allele num: 118316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431379
  ensembl transcript: ENST00000488246
  gene symbol: TATDN3
  hgvsc: ENST00000488246.2:c.256+7_256+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000497768
  gene symbol: TATDN3
  hgvsc: ENST00000497768.3:n.251+7_251+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000436364
  ensembl transcript: ENST00000526997
  gene symbol: TATDN3
  hgvsc: ENST00000526997.1:c.258+7_258+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355941
  ensembl transcript: ENST00000366974
  gene symbol: TATDN3
  hgvsc: ENST00000366974.4:c.258+7_258+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000530392
  gene symbol: TATDN3
  hgvsc: ENST00000530392.1:n.302+7_302+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000431376
  ensembl transcript: ENST00000532324
  gene symbol: TATDN3
  hgvsc: ENST00000532324.1:c.258+7_258+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433755
  ensembl transcript: ENST00000531963
  gene symbol: TATDN3
  hgvsc: ENST00000531963.1:c.258+7_258+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434801
  ensembl transcript: ENST00000526641
  gene symbol: TATDN3
  hgvsc: ENST00000526641.1:c.258+7_258+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000475492
  ensembl transcript: ENST00000606486
  gene symbol: TATDN3
  hgvsc: ENST00000606486.1:c.72_74delGTC
  hgvsp: ENSP00000475492.1:p.Val25del
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000355940
  ensembl transcript: ENST00000366973
  gene symbol: TATDN3
  hgvsc: ENST00000366973.4:c.258+7_258+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000432730
  ensembl transcript: ENST00000530441
  gene symbol: TATDN3
  hgvsc: ENST00000530441.1:c.173+613_173+615delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl transcript: ENST00000525569
  gene symbol: TATDN3
  hgvsc: ENST00000525569.1:n.417+7_417+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434428
  ensembl transcript: ENST00000533650
  gene symbol: TATDN3
  hgvsc: ENST00000533650.1:c.258+7_258+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000434276
  ensembl transcript: ENST00000530399
  gene symbol: TATDN3
  hgvsc: ENST00000530399.2:c.255+7_255+9delGTC
  variant of: http://identifiers.org/hgnc/27010
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000203705
  ensembl protein: ENSP00000433143
  ensembl transcript: ENST00000525574
  gene symbol: TATDN3
  hgvsc: ENST00000525574.1:c.169+613_169+615delGTC
  variant of: http://identifiers.org/hgnc/27010
canonical: false
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27649
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val25del
num of homozygotes: 0
reference allele: AGTC

GenotypeDepth
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12762
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6552
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 875
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 484
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 306
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2982
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 229
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13672
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18027
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1055
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1290
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1792
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5775
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1727
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 4.86322188449848e-4
allele num: 16450
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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num of homozygotes: 0

Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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DP
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MQ
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QD
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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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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European (Finnish)
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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: 2
allele frequency: 3.013772942346524e-5
allele num: 66362
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

Latino
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MQRankSum
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SIO_000300: -8.54e-1

QD
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FS
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ReadPosRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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SIO_000300: -4.0e-4

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

East Asian
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Latino
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African
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 24964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.079e0

VQSLOD
type: SiteQuality
SIO_000300: -1.494e0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

MQ
type: SiteQuality
SIO_000300: 6.072e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

QD
type: SiteQuality
SIO_000300: 1.678e1

DP
type: SiteQuality
SIO_000300: 7.92268e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.79e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.77e-1

GenotypeDepth
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bin: 1.75e1
variant carriers: 2

GenotypeDepth
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bin: 3.75e1
variant carriers: 2

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 51
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variant carriers: 0

GenotypeDepth
all individuals: 2200
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variant carriers: 1

GenotypeQuality
all individuals: 398
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.75e1
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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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 1499
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1428
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3004
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26012
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 7.117437722419929e-4
allele num: 11240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2794
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.44e-1

QD
type: SiteQuality
SIO_000300: 1.076e1

FS
type: SiteQuality
SIO_000300: 1.2645e1

DP
type: SiteQuality
SIO_000300: 8.20273e5

MQ
type: SiteQuality
SIO_000300: 5.939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.151e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.92e-1

GenotypeDepth
all individuals: 34
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 225
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variant carriers: 0

GenotypeDepth
all individuals: 447
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variant carriers: 0

GenotypeDepth
all individuals: 33
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variant carriers: 0

GenotypeDepth
all individuals: 3959
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variant carriers: 1

GenotypeDepth
all individuals: 190
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GenotypeDepth
all individuals: 152
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GenotypeDepth
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GenotypeQuality
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bin: 2.75e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3152
bin: 3.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 1473
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 2.5e0
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GenotypeQuality
all individuals: 646
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variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1545
bin: 3.75e1
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GenotypeQuality
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3662
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.851851851851852e-3
allele num: 540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3956
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31668
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.35941e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e0

QD
type: SiteQuality
SIO_000300: 1.099e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQRankSum
type: SiteQuality
SIO_000300: -5.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.311e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.31e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

GenotypeDepth
all individuals: 1555
bin: 4.25e1
variant carriers: 1089

GenotypeDepth
all individuals: 14416
bin: 1.75e1
variant carriers: 10429

GenotypeDepth
all individuals: 2427
bin: 3.75e1
variant carriers: 1751

GenotypeDepth
all individuals: 89
bin: 8.25e1
variant carriers: 58

GenotypeDepth
all individuals: 1022
bin: 4.75e1
variant carriers: 726

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 131

GenotypeDepth
all individuals: 440
bin: 9.75e1
variant carriers: 302

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 48

GenotypeQuality
all individuals: 8124
bin: 2.5e0
variant carriers: 1301

GenotypeQuality
all individuals: 1631
bin: 7.25e1
variant carriers: 1236

GenotypeQuality
all individuals: 1966
bin: 3.25e1
variant carriers: 1410

GenotypeQuality
all individuals: 1583
bin: 7.75e1
variant carriers: 1222

GenotypeQuality
all individuals: 1916
bin: 5.25e1
variant carriers: 1349

GenotypeQuality
all individuals: 1425
bin: 8.25e1
variant carriers: 1102

GenotypeQuality
all individuals: 1838
bin: 5.75e1
variant carriers: 1307

GenotypeQuality
all individuals: 2073
bin: 2.75e1
variant carriers: 1464

GenotypeQuality
all individuals: 2285
bin: 7.5e0
variant carriers: 1618

GenotypeQuality
all individuals: 1968
bin: 4.25e1
variant carriers: 1368

GenotypeQuality
all individuals: 1934
bin: 1.25e1
variant carriers: 1429

GenotypeQuality
all individuals: 2033
bin: 1.75e1
variant carriers: 1524

GenotypeQuality
all individuals: 2033
bin: 3.75e1
variant carriers: 1399

GenotypeQuality
all individuals: 1429
bin: 9.25e1
variant carriers: 1196

GenotypeQuality
all individuals: 1937
bin: 4.75e1
variant carriers: 1361

GenotypeQuality
all individuals: 2244
bin: 2.25e1
variant carriers: 1597

GenotypeQuality
all individuals: 18581
bin: 9.75e1
variant carriers: 16472

GenotypeQuality
all individuals: 1754
bin: 6.75e1
variant carriers: 1273

GenotypeQuality
all individuals: 1471
bin: 8.75e1
variant carriers: 1177

GenotypeQuality
all individuals: 1698
bin: 6.25e1
variant carriers: 1237

European (Non-Finnish)
type: Population
allele count: 20022
allele frequency: 4.279851224830063e-1
allele num: 46782
num of homozygotes: 401

Other
type: Population
allele count: 278
allele frequency: 4.028985507246377e-1
allele num: 690
num of homozygotes: 9

East Asian
type: Population
allele count: 2122
allele frequency: 3.606390210740992e-1
allele num: 5884
num of homozygotes: 25

African
type: Population
allele count: 2379
allele frequency: 3.425979262672811e-1
allele num: 6944
num of homozygotes: 42

Latino
type: Population
allele count: 2510
allele frequency: 3.051300753707756e-1
allele num: 8226
num of homozygotes: 16

European (Finnish)
type: Population
allele count: 2388
allele frequency: 4.55030487804878e-1
allele num: 5248
num of homozygotes: 69

South Asian
type: Population
allele count: 5102
allele frequency: 4.038948701709943e-1
allele num: 12632
num of homozygotes: 48

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

QD
type: SiteQuality
SIO_000300: 7.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.819e-1

DP
type: SiteQuality
SIO_000300: 1.367562e6

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

MQ
type: SiteQuality
SIO_000300: 5.994e1

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 83

GenotypeDepth
all individuals: 11464
bin: 2.25e1
variant carriers: 2522

GenotypeDepth
all individuals: 650
bin: 5.25e1
variant carriers: 177

GenotypeDepth
all individuals: 4006
bin: 7.5e0
variant carriers: 252

GenotypeDepth
all individuals: 1022
bin: 4.75e1
variant carriers: 252

GenotypeDepth
all individuals: 440
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variant carriers: 126

GenotypeDepth
all individuals: 3953
bin: 3.25e1
variant carriers: 1047

GenotypeDepth
all individuals: 283
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variant carriers: 88

GenotypeQuality
all individuals: 1754
bin: 6.75e1
variant carriers: 476

GenotypeQuality
all individuals: 8124
bin: 2.5e0
variant carriers: 426

GenotypeQuality
all individuals: 1583
bin: 7.75e1
variant carriers: 359

GenotypeQuality
all individuals: 2033
bin: 1.75e1
variant carriers: 488

GenotypeQuality
all individuals: 1429
bin: 9.25e1
variant carriers: 229

GenotypeQuality
all individuals: 1966
bin: 3.25e1
variant carriers: 608

GenotypeQuality
all individuals: 2033
bin: 3.75e1
variant carriers: 638

GenotypeQuality
all individuals: 2285
bin: 7.5e0
variant carriers: 524

GenotypeQuality
all individuals: 1916
bin: 5.25e1
variant carriers: 597

GenotypeQuality
all individuals: 1698
bin: 6.25e1
variant carriers: 451

GenotypeQuality
all individuals: 2244
bin: 2.25e1
variant carriers: 522

GenotypeQuality
all individuals: 1471
bin: 8.75e1
variant carriers: 298

GenotypeQuality
all individuals: 2073
bin: 2.75e1
variant carriers: 621

GenotypeQuality
all individuals: 1934
bin: 1.25e1
variant carriers: 441

GenotypeQuality
all individuals: 1937
bin: 4.75e1
variant carriers: 576

GenotypeQuality
all individuals: 1968
bin: 4.25e1
variant carriers: 600

GenotypeQuality
all individuals: 1631
bin: 7.25e1
variant carriers: 386

GenotypeQuality
all individuals: 18581
bin: 9.75e1
variant carriers: 2146

GenotypeQuality
all individuals: 1425
bin: 8.25e1
variant carriers: 319

GenotypeQuality
all individuals: 1838
bin: 5.75e1
variant carriers: 576

East Asian
type: Population
allele count: 830
allele frequency: 1.410605030591434e-1
allele num: 5884
num of homozygotes: 0

Other
type: Population
allele count: 74
allele frequency: 1.072463768115942e-1
allele num: 690
num of homozygotes: 0

South Asian
type: Population
allele count: 1254
allele frequency: 9.927169094363521e-2
allele num: 12632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 303
allele frequency: 5.773628048780488e-2
allele num: 5248
num of homozygotes: 0

African
type: Population
allele count: 1229
allele frequency: 1.769873271889401e-1
allele num: 6944
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 3923
allele frequency: 8.385703903210637e-2
allele num: 46782
num of homozygotes: 0

Latino
type: Population
allele count: 1575
allele frequency: 1.914660831509847e-1
allele num: 8226
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.819e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

QD
type: SiteQuality
SIO_000300: 7.35e0

MQ
type: SiteQuality
SIO_000300: 5.994e1

DP
type: SiteQuality
SIO_000300: 1.367562e6

GenotypeDepth
all individuals: 152
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2427
bin: 3.75e1
variant carriers: 60

GenotypeDepth
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7014
bin: 2.75e1
variant carriers: 159

GenotypeDepth
all individuals: 399
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GenotypeDepth
all individuals: 63
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variant carriers: 1

GenotypeDepth
all individuals: 1022
bin: 4.75e1
variant carriers: 21

GenotypeDepth
all individuals: 440
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variant carriers: 5

GenotypeQuality
all individuals: 1966
bin: 3.25e1
variant carriers: 91

GenotypeQuality
all individuals: 1754
bin: 6.75e1
variant carriers: 35

GenotypeQuality
all individuals: 2033
bin: 3.75e1
variant carriers: 90

GenotypeQuality
all individuals: 1934
bin: 1.25e1
variant carriers: 117

GenotypeQuality
all individuals: 1425
bin: 8.25e1
variant carriers: 27

GenotypeQuality
all individuals: 2244
bin: 2.25e1
variant carriers: 134

GenotypeQuality
all individuals: 8124
bin: 2.5e0
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GenotypeQuality
all individuals: 1698
bin: 6.25e1
variant carriers: 37

GenotypeQuality
all individuals: 1916
bin: 5.25e1
variant carriers: 80

GenotypeQuality
all individuals: 2073
bin: 2.75e1
variant carriers: 140

GenotypeQuality
all individuals: 1471
bin: 8.75e1
variant carriers: 18

GenotypeQuality
all individuals: 1937
bin: 4.75e1
variant carriers: 73

GenotypeQuality
all individuals: 1631
bin: 7.25e1
variant carriers: 36

GenotypeQuality
all individuals: 1968
bin: 4.25e1
variant carriers: 93

GenotypeQuality
all individuals: 2033
bin: 1.75e1
variant carriers: 112

GenotypeQuality
all individuals: 2285
bin: 7.5e0
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GenotypeQuality
all individuals: 1838
bin: 5.75e1
variant carriers: 49

GenotypeQuality
all individuals: 18581
bin: 9.75e1
variant carriers: 99

GenotypeQuality
all individuals: 1583
bin: 7.75e1
variant carriers: 24

GenotypeQuality
all individuals: 1429
bin: 9.25e1
variant carriers: 16

East Asian
type: Population
allele count: 45
allele frequency: 7.647858599592114e-3
allele num: 5884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 53
allele frequency: 1.009908536585366e-2
allele num: 5248
num of homozygotes: 0

Other
type: Population
allele count: 11
allele frequency: 1.594202898550725e-2
allele num: 690
num of homozygotes: 0

African
type: Population
allele count: 52
allele frequency: 7.488479262672811e-3
allele num: 6944
num of homozygotes: 0

South Asian
type: Population
allele count: 242
allele frequency: 1.915769474350855e-2
allele num: 12632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 518
allele frequency: 1.10726347740584e-2
allele num: 46782
num of homozygotes: 0

Latino
type: Population
allele count: 38
allele frequency: 4.61949914903963e-3
allele num: 8226
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.994e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.819e-1

QD
type: SiteQuality
SIO_000300: 7.35e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

DP
type: SiteQuality
SIO_000300: 1.367562e6

GenotypeDepth
all individuals: 11464
bin: 2.25e1
variant carriers: 8

GenotypeDepth
all individuals: 3953
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 650
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GenotypeDepth
all individuals: 152
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GenotypeDepth
all individuals: 440
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GenotypeDepth
all individuals: 63
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GenotypeDepth
all individuals: 1555
bin: 4.25e1
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GenotypeDepth
all individuals: 89
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GenotypeQuality
all individuals: 1968
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variant carriers: 3

GenotypeQuality
all individuals: 2244
bin: 2.25e1
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GenotypeQuality
all individuals: 1583
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1937
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2033
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1966
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1698
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 8124
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 2285
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 1429
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1934
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1754
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1916
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 18581
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2073
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1471
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2033
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1425
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1838
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 5.716463414634146e-4
allele num: 5248
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.449275362318841e-3
allele num: 690
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.699524133242692e-4
allele num: 5884
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.880184331797235e-4
allele num: 6944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.923816852635629e-4
allele num: 46782
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.749841671944268e-4
allele num: 12632
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.215657670799903e-4
allele num: 8226
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.819e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

QD
type: SiteQuality
SIO_000300: 7.35e0

DP
type: SiteQuality
SIO_000300: 1.367562e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

MQ
type: SiteQuality
SIO_000300: 5.994e1

GenotypeDepth
all individuals: 283
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 1555
bin: 4.25e1
variant carriers: 12

GenotypeDepth
all individuals: 440
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14416
bin: 1.75e1
variant carriers: 113

GenotypeDepth
all individuals: 2427
bin: 3.75e1
variant carriers: 24

GenotypeDepth
all individuals: 112
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 7.25e1
variant carriers: 14

GenotypeQuality
all individuals: 1934
bin: 1.25e1
variant carriers: 33

GenotypeQuality
all individuals: 18581
bin: 9.75e1
variant carriers: 31

GenotypeQuality
all individuals: 1754
bin: 6.75e1
variant carriers: 15

GenotypeQuality
all individuals: 2073
bin: 2.75e1
variant carriers: 27

GenotypeQuality
all individuals: 2244
bin: 2.25e1
variant carriers: 32

GenotypeQuality
all individuals: 1966
bin: 3.25e1
variant carriers: 32

GenotypeQuality
all individuals: 2033
bin: 1.75e1
variant carriers: 26

GenotypeQuality
all individuals: 1429
bin: 9.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1698
bin: 6.25e1
variant carriers: 23

GenotypeQuality
all individuals: 1916
bin: 5.25e1
variant carriers: 15

GenotypeQuality
all individuals: 8124
bin: 2.5e0
variant carriers: 33

GenotypeQuality
all individuals: 1968
bin: 4.25e1
variant carriers: 24

GenotypeQuality
all individuals: 2285
bin: 7.5e0
variant carriers: 54

GenotypeQuality
all individuals: 1583
bin: 7.75e1
variant carriers: 16

GenotypeQuality
all individuals: 1471
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2033
bin: 3.75e1
variant carriers: 28

GenotypeQuality
all individuals: 1937
bin: 4.75e1
variant carriers: 25

GenotypeQuality
all individuals: 1838
bin: 5.75e1
variant carriers: 21

GenotypeQuality
all individuals: 1425
bin: 8.25e1
variant carriers: 18

European (Finnish)
type: Population
allele count: 11
allele frequency: 2.096036585365854e-3
allele num: 5248
num of homozygotes: 0

East Asian
type: Population
allele count: 41
allele frequency: 6.968048946295037e-3
allele num: 5884
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 7.246376811594203e-3
allele num: 690
num of homozygotes: 0

African
type: Population
allele count: 38
allele frequency: 5.472350230414746e-3
allele num: 6944
num of homozygotes: 0

Latino
type: Population
allele count: 51
allele frequency: 6.199854121079504e-3
allele num: 8226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 137
allele frequency: 2.928476764567569e-3
allele num: 46782
num of homozygotes: 0

South Asian
type: Population
allele count: 47
allele frequency: 3.720709309689677e-3
allele num: 12632
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

MQ
type: SiteQuality
SIO_000300: 5.994e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

DP
type: SiteQuality
SIO_000300: 1.367562e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.819e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

QD
type: SiteQuality
SIO_000300: 7.35e0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.412722842118764e-5
allele num: 46782
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.583280557314756e-4
allele num: 12632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.367562e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.819e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

MQ
type: SiteQuality
SIO_000300: 5.994e1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

QD
type: SiteQuality
SIO_000300: 7.35e0

GenotypeDepth
all individuals: 85
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 978
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1791
bin: 4.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 614
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9026
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 174
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 304
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 344
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1038
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8502
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34747
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2998
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4217
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 397
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.029385034837928e-4
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.984672223748893e-4
allele num: 65502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

MQRankSum
type: SiteQuality
SIO_000300: -3.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 1.794748e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.447e1

GenotypeDepth
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 20675
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19086
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9093
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 805
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variant carriers: 0

GenotypeDepth
all individuals: 1793
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3638
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 979
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4205
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34706
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3005
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3349
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2012
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65740
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.102770657878677e-5
allele num: 16386
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.802515e6

VQSLOD
type: SiteQuality
SIO_000300: 3.38e-1

FS
type: SiteQuality
SIO_000300: 3.491e0

MQRankSum
type: SiteQuality
SIO_000300: -1.216e0

QD
type: SiteQuality
SIO_000300: 1.35e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

GenotypeDepth
all individuals: 700
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 257
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 342
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 979
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 493
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 304
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 613
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9141
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35432
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8561
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3003
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4214
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9942
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.100536847242558e-5
allele num: 16392
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.04e-1

DP
type: SiteQuality
SIO_000300: 1.808093e6

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.421e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 9.624000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.893e1

GenotypeDepth
all individuals: 20863
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 700
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 19203
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9141
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 257
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variant carriers: 0

GenotypeDepth
all individuals: 85
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variant carriers: 0

GenotypeDepth
all individuals: 716
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1797
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 342
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variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 231
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35432
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3003
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8561
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 134
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 226
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4214
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3351
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517634917744187e-5
allele num: 65892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.808093e6

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.893e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

FS
type: SiteQuality
SIO_000300: 9.624000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.04e-1

QD
type: SiteQuality
SIO_000300: 1.421e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

GenotypeDepth
all individuals: 304
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 343
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1800
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 49
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 663
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variant carriers: 0

GenotypeDepth
all individuals: 655
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variant carriers: 0

GenotypeDepth
all individuals: 85
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variant carriers: 0

GenotypeDepth
all individuals: 714
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19273
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 613
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variant carriers: 0

GenotypeDepth
all individuals: 162
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variant carriers: 0

GenotypeQuality
all individuals: 8574
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variant carriers: 0

GenotypeQuality
all individuals: 960
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 1044
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GenotypeQuality
all individuals: 2014
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 35666
bin: 6.25e1
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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.515978412467406e-5
allele num: 65964
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

DP
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SIO_000300: 1.810489e6

BaseQRankSum
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SIO_000300: -2.319e0

MQRankSum
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SIO_000300: 2.34e-1

ClippingRankSum
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SIO_000300: -1.053e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
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SIO_000300: 5.996e1

VQSLOD
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SIO_000300: 4.83e0

QD
type: SiteQuality
SIO_000300: 1.685e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

GenotypeDepth
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variant carriers: 16

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

East Asian
type: Population
allele count: 3
allele frequency: 3.480278422273782e-4
allele num: 8620
num of homozygotes: 0

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

African
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allele count: 13
allele frequency: 1.327072274397713e-3
allele num: 9796
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.682062858135092e-5
allele num: 11518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 10
allele frequency: 1.54273372415921e-3
allele num: 6482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 50
allele frequency: 7.631490582740621e-4
allele num: 65518
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.43e0

FS
type: SiteQuality
SIO_000300: 8.2541e1

InbreedingCoeff
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SIO_000300: -2.5e-3

BaseQRankSum
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SIO_000300: -3.634e0

MQ
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SIO_000300: 5.958e1

ReadPosRankSum
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SIO_000300: -1.738e0

DP
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SIO_000300: 1.830642e6

VQSLOD
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SIO_000300: -3.436e1

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

QD
type: SiteQuality
SIO_000300: 2.8e-1

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

South Asian
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allele count: 4
allele frequency: 2.438726984514084e-4
allele num: 16402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.535284513515148e-5
allele num: 66148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

ClippingRankSum
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SIO_000300: -3.88e-1

FS
type: SiteQuality
SIO_000300: 5.93e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.14e1

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

DP
type: SiteQuality
SIO_000300: 1.823081e6

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.022974607013301e-5
allele num: 66160
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.094588005850804e-5
allele num: 16408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 92
allele frequency: 9.146947703320739e-3
allele num: 10058
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.734304543877905e-4
allele num: 11532
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.88e0

DP
type: SiteQuality
SIO_000300: 1.826063e6

BaseQRankSum
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SIO_000300: 1.61e0

FS
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QD
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SIO_000300: 1.213e1

ClippingRankSum
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SIO_000300: -3.35e-1

MQ
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SIO_000300: 5.96e1

InbreedingCoeff
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SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.510528382828313e-5
allele num: 66202
num of homozygotes: 0

ReadPosRankSum
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MQ
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DP
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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East Asian
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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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European (Non-Finnish)
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allele frequency: 1.509889778046203e-5
allele num: 66230
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European (Finnish)
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allele count: 0
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 2.967359050445104e-4
allele num: 10110
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66250
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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East Asian
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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MQRankSum
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DP
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MQ
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ClippingRankSum
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QD
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VQSLOD
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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South Asian
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num of homozygotes: 0

East 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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Latino
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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SIO_000300: -6.57e-1

InbreedingCoeff
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QD
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MQ
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FS
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VQSLOD
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DP
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GenotypeDepth
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variant carriers: 3

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

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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Latino
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allele num: 11542
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European (Finnish)
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African
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allele num: 10152
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Other
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South Asian
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InbreedingCoeff
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BaseQRankSum
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QD
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MQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66380
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South Asian
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European (Finnish)
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Latino
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African
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East Asian
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Other
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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FS
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Non-Finnish)
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African
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Latino
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South Asian
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European (Finnish)
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ClippingRankSum
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QD
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DP
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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East Asian
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South Asian
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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South Asian
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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Latino
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European (Non-Finnish)
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Other
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BaseQRankSum
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QD
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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South Asian
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African
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MQRankSum
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FS
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InbreedingCoeff
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DP
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MQ
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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Latino
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Other
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European (Finnish)
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African
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FS
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DP
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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MQ
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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VQSLOD
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MQ
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BaseQRankSum
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DP
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MQRankSum
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FS
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ReadPosRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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VQSLOD
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InbreedingCoeff
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FS
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QD
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MQ
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ReadPosRankSum
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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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East 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 frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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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 frequency: 1.524762137106611e-5
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num of homozygotes: 0

InbreedingCoeff
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MQ
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DP
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MQRankSum
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

African
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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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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.079765937788728e-5
allele num: 64940
num of homozygotes: 0

DP
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BaseQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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InbreedingCoeff
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SIO_000300: 2.9e-3

MQRankSum
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QD
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SIO_000300: 1.58e1

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

South Asian
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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: 1.539882968894364e-5
allele num: 64940
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.193e0

MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 2.9e-3

QD
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SIO_000300: 1.58e1

DP
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SIO_000300: 1.488184e6

GenotypeDepth
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variant carriers: 3

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.113964294448521e-5
allele num: 65424
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.231830500123183e-4
allele num: 16236
num of homozygotes: 0

African
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allele count: 31
allele frequency: 3.022031585104309e-3
allele num: 10258
num of homozygotes: 0

Other
type: Population
allele count: 0
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num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 3.54735721887194e-4
allele num: 11276
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 1.4e-3

FS
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SIO_000300: 0.0e0

BaseQRankSum
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VQSLOD
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DP
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ClippingRankSum
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QD
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MQRankSum
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SIO_000300: 6.66e-1

ReadPosRankSum
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SIO_000300: -6.7e-2

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65344
num of homozygotes: 0

European (Finnish)
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African
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Latino
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South Asian
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Other
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East Asian
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VQSLOD
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MQ
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DP
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ClippingRankSum
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QD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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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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BaseQRankSum
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FS
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MQRankSum
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QD
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Other
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South Asian
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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

African
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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: 1.517773123273533e-5
allele num: 65886
num of homozygotes: 0

FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -3.0e-4

DP
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.515013786625458e-5
allele num: 66006
num of homozygotes: 0

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

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

FS
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SIO_000300: 1.704e0

BaseQRankSum
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MQRankSum
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MQ
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VQSLOD
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QD
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DP
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 9.659969088098918e-5
allele num: 10352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.796622097114708e-5
allele num: 11368
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66064
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 3.75e0

FS
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SIO_000300: 1.54e0

ClippingRankSum
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SIO_000300: -6.8e-1

InbreedingCoeff
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VQSLOD
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SIO_000300: -8.764999999999999e-1

MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 1.86e0

ReadPosRankSum
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SIO_000300: 4.79e-1

QD
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SIO_000300: 1.692e1

DP
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SIO_000300: 1.595028e6

GenotypeDepth
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512447442451375e-5
allele num: 66118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.83e-1

DP
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QD
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SIO_000300: 1.282e1

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: -1.112e0

MQ
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SIO_000300: 6.0e1

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -1.365e0

MQRankSum
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SIO_000300: 6.1e-2

GenotypeDepth
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variant carriers: 171

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 21
allele frequency: 2.333333333333333e-2
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 94
allele frequency: 1.430310407790627e-2
allele num: 6572
num of homozygotes: 0

Latino
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allele count: 139
allele frequency: 1.219512195121951e-2
allele num: 11398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2146
allele frequency: 3.241691842900302e-2
allele num: 66200
num of homozygotes: 47

East Asian
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allele count: 150
allele frequency: 1.741351288599954e-2
allele num: 8614
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African
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allele count: 57
allele frequency: 5.500868558193399e-3
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South Asian
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allele count: 255
allele frequency: 1.555636896046852e-2
allele num: 16392
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MQ
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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QD
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SIO_000300: 1.406e1

InbreedingCoeff
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SIO_000300: 1.84e-2

DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66200
num of homozygotes: 0

East Asian
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allele count: 0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
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South Asian
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MQRankSum
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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
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Latino
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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
allele num: 6580
num of homozygotes: 0

InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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DP
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 3.013046491307361e-5
allele num: 66378
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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 frequency: 0.0e0
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East Asian
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VQSLOD
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InbreedingCoeff
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QD
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BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6590
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 count: 0
allele frequency: 0.0e0
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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.50652324565368e-5
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num of homozygotes: 0

African
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BaseQRankSum
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MQ
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66430
num of homozygotes: 0

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

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

Other
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QD
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MQRankSum
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DP
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BaseQRankSum
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FS
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SIO_000300: 0.0e0

InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16446
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Latino
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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MQRankSum
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DP
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VQSLOD
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MQ
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ReadPosRankSum
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

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

Other
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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: 6.001680470531749e-5
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East Asian
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African
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Latino
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQ
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VQSLOD
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9
allele frequency: 8.65884163940735e-4
allele num: 10394
num of homozygotes: 0

Other
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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

East Asian
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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
allele num: 66650
num of homozygotes: 0

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

South Asian
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQ
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DP
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QD
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MQRankSum
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FS
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InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 66496
num of homozygotes: 0

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: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

Latino
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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: 16444
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
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QD
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BaseQRankSum
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SIO_000300: -4.21e-1

MQRankSum
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SIO_000300: -7.75e-1

VQSLOD
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ClippingRankSum
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DP
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SIO_000300: 1.604939e6

ReadPosRankSum
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FS
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SIO_000300: 3.473e0

MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
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: 3
allele frequency: 4.514129224472599e-5
allele num: 66458
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

FS
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SIO_000300: 2.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

QD
type: SiteQuality
SIO_000300: 1.609e1

DP
type: SiteQuality
SIO_000300: 1.603719e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66362
num of homozygotes: 0

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

South Asian
type: Population
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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
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SIO_000300: 1.201e0

ClippingRankSum
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SIO_000300: -1.103e0

BaseQRankSum
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MQ
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ReadPosRankSum
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QD
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DP
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VQSLOD
type: SiteQuality
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MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
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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South Asian
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African
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Latino
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allele count: 0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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ReadPosRankSum
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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DP
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MQRankSum
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MQ
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SIO_000300: 5.886e1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.306e1

GenotypeDepth
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variant carriers: 17

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 8
allele frequency: 7.011393514460999e-4
allele num: 11410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 111
allele frequency: 1.683246390877108e-3
allele num: 65944
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European (Finnish)
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African
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South Asian
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allele count: 94
allele frequency: 5.758392550845381e-3
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Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
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FS
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ClippingRankSum
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QD
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.48e-2

DP
type: SiteQuality
SIO_000300: 1.598888e6

GenotypeDepth
all individuals: 1054
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1049
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 585
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 422
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 139
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 139
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 921
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47501
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 427
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5624
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 8.75e1
variant carriers: 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: 8
allele frequency: 4.927322000492732e-4
allele num: 16236
num of homozygotes: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
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: 1
allele frequency: 1.525646111128063e-5
allele num: 65546
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.456e1

VQSLOD
type: SiteQuality
SIO_000300: 4.82e0

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.93e-2

DP
type: SiteQuality
SIO_000300: 1.583373e6

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

GenotypeDepth
all individuals: 1528
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1041
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 20323
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 430
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 421
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5521
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46037
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 423
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2882
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2123
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1019
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541829843658454e-5
allele num: 64858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16066
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

FS
type: SiteQuality
SIO_000300: 4.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.669e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 1.566333e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e-1

QD
type: SiteQuality
SIO_000300: 1.775e1

GenotypeDepth
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 20323
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 282
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1041
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 75
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 361
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 583
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1703
bin: 1.25e1
variant carriers: 0