19-6741304-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6741304
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6741304
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 72886
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.57+12G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.197+12G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.197+12G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-128+12G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.274+12G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.197+12G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.500+12G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.338+12G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.197+12G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.430+12G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-128+168G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.232+12G>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20096
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

19-6741306-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6741306
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6741306
    reference: chr 19
allele count: 41
allele frequency: 5.840622239949856e-4
allele num: 70198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.338+14G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.57+14G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.197+14G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.430+14G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.274+14G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-128+170G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-128+14G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.232+14G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.197+14G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.500+14G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.197+14G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.197+14G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20154
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19732
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-6741326-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6741326
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6741326
    reference: chr 19
allele count: 3
allele frequency: 5.415748998086435e-5
allele num: 55394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.232+34G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.500+34G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.430+34G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.197+34G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-128+34G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.197+34G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.338+34G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.197+34G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-128+190G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.197+34G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.274+34G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.57+34G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21944
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15643
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10068
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

19-6741330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6741330
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6741330
    reference: chr 19
allele count: 1
allele frequency: 1.914975105323631e-5
allele num: 52220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.338+38G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.197+38G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.197+38G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-128+194G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.430+38G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.197+38G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.274+38G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.57+38G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-128+38G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.500+38G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.232+38G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.197+38G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10553
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14286
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-6741337-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6741337
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6741337
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 45310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.197+45C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-128+45C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.197+45C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.232+45C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.430+45C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.197+45C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.57+45C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.338+45C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.274+45C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.197+45C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-128+201C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.500+45C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25912
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10949
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

19-6741340-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6741340
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6741340
    reference: chr 19
allele count: 2
allele frequency: 4.638434064659771e-5
allele num: 43118
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.197+48T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.197+48T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.338+48T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.232+48T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.197+48T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.57+48T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.197+48T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-128+48T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.500+48T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.274+48T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-128+204T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.430+48T>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26787
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11057
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10174
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

19-6741344-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6741344
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6741344
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 41588
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.338+52T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.197+52T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.57+52T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.197+52T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.430+52T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.197+52T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-128+52T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.274+52T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-128+208T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.197+52T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.232+52T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.500+52T>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26871
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11086
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

19-6742929-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742929
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742929
    reference: chr 19
allele count: 25
allele frequency: 2.10817465805407e-4
allele num: 118586
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-49C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-49C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-49C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-49C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-49C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-49C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-49C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-49C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-49C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-49C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-49C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-49C>G
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 28810
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

19-6742929-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742929
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742929
    reference: chr 19
allele count: 1
allele frequency: 8.432698632216282e-6
allele num: 118586
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-49C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-49C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-49C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-49C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-49C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-49C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-49C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-49C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-49C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-49C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-49C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-49C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-6742930-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742930
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742930
    reference: chr 19
allele count: 3
allele frequency: 2.525337553452978e-5
allele num: 118796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-48G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-48G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-48G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-48G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-48G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-48G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-48G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-48G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-48G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-48G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-48G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-48G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-6742937-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742937
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742937
    reference: chr 19
allele count: 1
allele frequency: 8.405197774303629e-6
allele num: 118974
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-41G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-41G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-41G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-41G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-41G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-41G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-41G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-41G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-41G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-41G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-41G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-41G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

19-6742946-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742946
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742946
    reference: chr 19
allele count: 2
allele frequency: 1.678162076893386e-5
allele num: 119178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-32C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-32C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-32C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-32C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-32C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-32C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-32C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-32C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-32C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-32C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-32C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-32C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-6742951-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742951
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742951
    reference: chr 19
allele count: 1
allele frequency: 8.367080558251614e-6
allele num: 119516
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-27T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-27T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-27T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-27T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-27T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-27T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-27T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-27T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-27T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-27T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-27T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-27T>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP

19-6742955-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742955
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742955
    reference: chr 19
allele count: 108
allele frequency: 9.024064171122995e-4
allele num: 119680
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-23C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-23C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-23C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-23C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-23C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-23C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-23C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-23C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-23C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-23C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-23C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-23C>G
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14007
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 29510
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10679
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS

19-6742955-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742955
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742955
    reference: chr 19
allele count: 14
allele frequency: 1.169786096256684e-4
allele num: 119680
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-23C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-23C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-23C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-23C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-23C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-23C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-23C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-23C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-23C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-23C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-23C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-23C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10679
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

19-6742955-CCCCGATTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742955
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742946
    reference: chr 19
allele count: 1
allele frequency: 8.355614973262032e-6
allele num: 119680
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: CCCCGATTCT
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-6742958-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742958
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742958
    reference: chr 19
allele count: 2
allele frequency: 1.668864004272292e-5
allele num: 119842
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-20C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-20C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-20C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-20C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-20C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-20C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-20C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-20C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-20C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-20C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-20C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-20C>G
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10745
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-6742958-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742958
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742958
    reference: chr 19
allele count: 8
allele frequency: 6.675456017089168e-5
allele num: 119842
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-20C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-20C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-20C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-20C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-20C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-20C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-20C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-20C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-20C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-20C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-20C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-20C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29664
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

19-6742959-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742959
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742959
    reference: chr 19
allele count: 3
allele frequency: 2.499458450669022e-5
allele num: 120026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-19G>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10752
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-6742966-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742966
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742966
    reference: chr 19
allele count: 1
allele frequency: 8.297653423611802e-6
allele num: 120516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-12A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-12A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-12A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-12A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-12A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-12A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-12A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-12A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-12A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-12A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-12A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-12A>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10811
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-6742973-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742973
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742973
    reference: chr 19
allele count: 1
allele frequency: 8.275953389830508e-6
allele num: 120832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.501-5C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.233-5C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.58-5C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.198-5C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.198-5C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.275-5C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.339-5C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-127-5C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-127-5C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.198-5C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.431-5C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.198-5C>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30163
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14834
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.198-5C>A
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

19-6742979-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742979
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742979
    reference: chr 19
allele count: 39
allele frequency: 3.222661091738419e-4
allele num: 121018
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.199T>C
  hgvsp: ENSP00000472580.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.199T>C
  hgvsp: ENSP00000320117.7:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.276T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-126T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.199T>C
  hgvsp: ENSP00000469360.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.340T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.199T>C
  hgvsp: ENSP00000320493.6:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-126T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.502T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.234T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.432T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.59T>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10934
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14881
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Phe67Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

19-6742983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742983
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742983
    reference: chr 19
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-122G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.344G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.203G>A
  hgvsp: ENSP00000320493.6:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.203G>A
  hgvsp: ENSP00000320117.7:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.203G>A
  hgvsp: ENSP00000469360.1:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.203G>A
  hgvsp: ENSP00000472580.1:p.Ser68Asn
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.63G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.238G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.506G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-122G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.280G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.436G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10970
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser68Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

19-6742999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6742999
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6742999
    reference: chr 19
allele count: 93
allele frequency: 7.665298452104248e-4
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.79C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-106C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.296C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.254C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-106C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.219C>T
  hgvsp: ENST00000596758.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.219C>T
  hgvsp: ENST00000600677.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.360C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.452C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.522C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.219C>T
  hgvsp: ENST00000313244.9:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.219C>T
  hgvsp: ENST00000313285.8:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11020
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30569
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14842
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Phe73Phe
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

19-6743000-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743000
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743000
    reference: chr 19
allele count: 16
allele frequency: 1.318674073219378e-4
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.297G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.523G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.80G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.220G>A
  hgvsp: ENSP00000469360.1:p.Val74Ile
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.220G>A
  hgvsp: ENSP00000472580.1:p.Val74Ile
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.453G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.361G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.220G>A
  hgvsp: ENSP00000320493.6:p.Val74Ile
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-105G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.255G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-105G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.220G>A
  hgvsp: ENSP00000320117.7:p.Val74Ile
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val74Ile
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: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

19-6743004-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743004
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743004
    reference: chr 19
allele count: 2
allele frequency: 1.648043772042586e-5
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.224A>T
  hgvsp: ENSP00000472580.1:p.Gln75Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.457A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.224A>T
  hgvsp: ENSP00000320493.6:p.Gln75Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-101A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.365A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.259A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-101A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.224A>T
  hgvsp: ENSP00000469360.1:p.Gln75Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.527A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.224A>T
  hgvsp: ENSP00000320117.7:p.Gln75Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.301A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.84A>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln75Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP

19-6743020-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743020
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743020
    reference: chr 19
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.543G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.381G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.473G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.240G>C
  hgvsp: ENST00000313244.9:c.240G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.240G>C
  hgvsp: ENST00000596758.1:c.240G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.100G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.317G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.275G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.240G>C
  hgvsp: ENST00000600677.1:c.240G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.240G>C
  hgvsp: ENST00000313285.8:c.240G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-85G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-85G>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val80Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-6743023-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743023
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743023
    reference: chr 19
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.384T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.243T>C
  hgvsp: ENST00000596758.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.243T>C
  hgvsp: ENST00000313244.9:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-82T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.243T>C
  hgvsp: ENST00000313285.8:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-82T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.320T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.546T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.278T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.243T>C
  hgvsp: ENST00000600677.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.476T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.103T>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn81Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

19-6743024-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743024
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743024
    reference: chr 19
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.547G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.244G>A
  hgvsp: ENSP00000472580.1:p.Asp82Asn
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-81G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.321G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-81G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.385G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.104G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.244G>A
  hgvsp: ENSP00000320117.7:p.Asp82Asn
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.244G>A
  hgvsp: ENSP00000469360.1:p.Asp82Asn
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.279G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.477G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.244G>A
  hgvsp: ENSP00000320493.6:p.Asp82Asn
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp82Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

19-6743046-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743046
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743046
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.266T>C
  hgvsp: ENSP00000472580.1:p.Leu89Pro
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.266T>C
  hgvsp: ENSP00000320493.6:p.Leu89Pro
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.343T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.569T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.266T>C
  hgvsp: ENSP00000320117.7:p.Leu89Pro
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-59T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.301T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.266T>C
  hgvsp: ENSP00000469360.1:p.Leu89Pro
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.126T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-59T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.499T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.407T>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu89Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

19-6743048-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743048
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743048
    reference: chr 19
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-57G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.501G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.571G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.268G>A
  hgvsp: ENSP00000472580.1:p.Val90Met
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-57G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.128G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.345G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.303G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.268G>A
  hgvsp: ENSP00000469360.1:p.Val90Met
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.268G>A
  hgvsp: ENSP00000320117.7:p.Val90Met
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.409G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.268G>A
  hgvsp: ENSP00000320493.6:p.Val90Met
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val90Met
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

19-6743048-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743048
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743048
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-57G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.268G>C
  hgvsp: ENSP00000320117.7:p.Val90Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-57G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.128G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.409G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.303G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.268G>C
  hgvsp: ENSP00000472580.1:p.Val90Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.345G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.268G>C
  hgvsp: ENSP00000469360.1:p.Val90Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.268G>C
  hgvsp: ENSP00000320493.6:p.Val90Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.501G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.571G>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val90Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum

19-6743069-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743069
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743069
    reference: chr 19
allele count: 3
allele frequency: 2.47133254250692e-5
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.324C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.366C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.289C>T
  hgvsp: ENSP00000472580.1:p.Arg97Cys
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-36C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.289C>T
  hgvsp: ENSP00000320117.7:p.Arg97Cys
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.289C>T
  hgvsp: ENSP00000469360.1:p.Arg97Cys
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-36C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.149C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.289C>T
  hgvsp: ENSP00000320493.6:p.Arg97Cys
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.592C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.522C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.430C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11061
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg97Cys
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-6743070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743070
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743070
    reference: chr 19
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.290G>A
  hgvsp: ENSP00000469360.1:p.Arg97His
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.523G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.593G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.290G>A
  hgvsp: ENSP00000320117.7:p.Arg97His
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.367G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.290G>A
  hgvsp: ENSP00000472580.1:p.Arg97His
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.431G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.150G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.290G>A
  hgvsp: ENSP00000320493.6:p.Arg97His
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.325G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg97His
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

19-6743079-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743079
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743079
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.299T>C
  hgvsp: ENSP00000320493.6:p.Leu100Pro
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.532T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.376T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.299T>C
  hgvsp: ENSP00000469360.1:p.Leu100Pro
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.602T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.299T>C
  hgvsp: ENSP00000320117.7:p.Leu100Pro
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.299T>C
  hgvsp: ENSP00000472580.1:p.Leu100Pro
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.159T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.440T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.334T>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu100Pro
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: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

19-6743086-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743086
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743086
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.539G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.447G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.609G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.306G>C
  hgvsp: ENST00000313244.9:c.306G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.306G>C
  hgvsp: ENST00000596758.1:c.306G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-19G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.306G>C
  hgvsp: ENST00000600677.1:c.306G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.383G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.341G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.306G>C
  hgvsp: ENST00000313285.8:c.306G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.166G>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu102Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-6743087-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743087
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743087
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.342A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-18A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.448A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.307A>G
  hgvsp: ENSP00000320117.7:p.Thr103Ala
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.307A>G
  hgvsp: ENSP00000469360.1:p.Thr103Ala
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.307A>G
  hgvsp: ENSP00000320493.6:p.Thr103Ala
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.610A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.384A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.167A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.540A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-18A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.307A>G
  hgvsp: ENSP00000472580.1:p.Thr103Ala
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr103Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

19-6743089-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743089
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743089
    reference: chr 19
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596543
  gene symbol: TRIP10
  hgvsc: ENST00000596543.1:n.542C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.169C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.309C>T
  hgvsp: ENST00000313285.8:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.450C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-16C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.612C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.344C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.309C>T
  hgvsp: ENST00000600677.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.309C>T
  hgvsp: ENST00000596758.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.309C>T
  hgvsp: ENST00000313244.9:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-16C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.386C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr103Thr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

19-6743096-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743096
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743096
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.-9T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.457T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.316T>A
  hgvsp: ENSP00000472580.1:p.Ser106Thr
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.176T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.393T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.-9T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.351T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.316T>A
  hgvsp: ENSP00000469360.1:p.Ser106Thr
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.316T>A
  hgvsp: ENSP00000320117.7:p.Ser106Thr
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.316T>A
  hgvsp: ENSP00000320493.6:p.Ser106Thr
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.619T>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser106Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

19-6743106-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743106
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743106
    reference: chr 19
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.361T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.403T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.2T>C
  hgvsp: ENSP00000471203.1:p.Met1?
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.326T>C
  hgvsp: ENSP00000320493.6:p.Met109Thr
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.326T>C
  hgvsp: ENSP00000469360.1:p.Met109Thr
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.629T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.467T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.2T>C
  hgvsp: ENSP00000471056.1:p.Met1?
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.326T>C
  hgvsp: ENSP00000472580.1:p.Met109Thr
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.326T>C
  hgvsp: ENSP00000320117.7:p.Met109Thr
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.186T>C
  variant of: http://identifiers.org/hgnc/12304
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-6743113-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743113
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743113
    reference: chr 19
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.9G>A
  hgvsp: ENST00000600428.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.333G>A
  hgvsp: ENST00000313244.9:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.193G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.333G>A
  hgvsp: ENST00000313285.8:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.333G>A
  hgvsp: ENST00000600677.1:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.368G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.9G>A
  hgvsp: ENST00000596673.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.333G>A
  hgvsp: ENST00000596758.1:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.474G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.636G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.410G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln111Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum

19-6743133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743133
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743133
    reference: chr 19
allele count: 3
allele frequency: 2.473003050037095e-5
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+8G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+8G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+8G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+8G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+8G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+8G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+8G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+8G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+8G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+8G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+8G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10827
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.345+8G>A
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

19-6743133-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743133
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743134
    reference: chr 19
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+14dupC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+14dupC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+14dupC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+14dupC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+14dupC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+14dupC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+14dupC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+14dupC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+14dupC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+14dupC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+14dupC
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14922
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

19-6743133-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743133
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743132
    reference: chr 19
allele count: 5
allele frequency: 4.121671750061825e-5
allele num: 121310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+14delC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+14delC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+14delC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+14delC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+14delC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+14delC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+14delC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+14delC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+14delC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+14delC
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+14delC
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30438
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8754
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: GC
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/19-6743134-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743134
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743134
    reference: chr 19
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+9C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+9C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+9C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+9C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+9C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+9C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+9C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+9C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+9C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+9C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+9C>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30436
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

19-6743134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743134
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743134
    reference: chr 19
allele count: 2
allele frequency: 1.649103712132456e-5
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+9C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+9C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+9C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+9C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+9C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+9C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+9C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+9C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+9C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+9C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+9C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

19-6743136-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743136
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743136
    reference: chr 19
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+11C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+11C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+11C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+11C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+11C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+11C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+11C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+11C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+11C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+11C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+11C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

19-6743139-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743139
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743139
    reference: chr 19
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+14C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+14C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+14C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+14C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+14C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+14C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+14C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+14C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+14C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+14C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+14C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP

19-6743140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743140
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743140
    reference: chr 19
allele count: 2
allele frequency: 1.64866870002473e-5
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+15G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+15G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+15G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+15G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+15G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+15G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+15G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+15G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+15G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+15G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+15G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

19-6743147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743147
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743147
    reference: chr 19
allele count: 4
allele frequency: 3.297663605335619e-5
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+22G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+22G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+22G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+22G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+22G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+22G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+22G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+22G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+22G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+22G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+22G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

19-6743151-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743151
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743151
    reference: chr 19
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+26T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+26T>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-6743154-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743154
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743154
    reference: chr 19
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+29A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+29A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+29A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+29A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+29A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+29A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+29A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+29A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+29A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+29A>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+29A>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

19-6743157-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743157
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743157
    reference: chr 19
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+32G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+32G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+32G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+32G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+32G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+32G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+32G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+32G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+32G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+32G>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+32G>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD

19-6743165-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743165
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743165
    reference: chr 19
allele count: 8
allele frequency: 6.596088519507932e-5
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.486+40G>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.21+40G>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.345+40G>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.205+40G>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.648+40G>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.422+40G>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.21+40G>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.345+40G>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.345+40G>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.345+40G>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.380+40G>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30461
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-6743173-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743173
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743173
    reference: chr 19
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.346-32C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.206-32C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.22-32C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.22-32C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.346-32C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.649-32C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.487-32C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.381-32C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.346-32C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.423-32C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.346-32C>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30646
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8599
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum

19-6743176-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743176
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743176
    reference: chr 19
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.649-29G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.346-29G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.346-29G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.22-29G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.22-29G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.423-29G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.346-29G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.487-29G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.346-29G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.206-29G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.381-29G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

19-6743178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743178
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743178
    reference: chr 19
allele count: 3
allele frequency: 2.474512521033356e-5
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.649-27C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.346-27C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.346-27C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.22-27C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.423-27C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.381-27C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.487-27C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.346-27C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.346-27C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.206-27C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.22-27C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

19-6743179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743179
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743179
    reference: chr 19
allele count: 3
allele frequency: 2.474512521033356e-5
allele num: 121236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.22-26G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.487-26G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.346-26G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.346-26G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.346-26G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.649-26G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.346-26G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.22-26G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.423-26G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.381-26G>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.206-26G>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

19-6743180-AGCCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743180
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743176
    reference: chr 19
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.381-24_381-21delGCCT
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.487-24_487-21delGCCT
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.346-24_346-21delGCCT
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.206-24_206-21delGCCT
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.346-24_346-21delGCCT
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.346-24_346-21delGCCT
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.22-24_22-21delGCCT
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.649-24_649-21delGCCT
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.423-24_423-21delGCCT
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.346-24_346-21delGCCT
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.22-24_22-21delGCCT
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: AGCCT
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

19-6743185-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743185
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743185
    reference: chr 19
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.381-20T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.346-20T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.346-20T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.423-20T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.22-20T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.487-20T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.649-20T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.346-20T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.206-20T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.346-20T>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.22-20T>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30729
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

19-6743190-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743190
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743190
    reference: chr 19
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.22-15C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.206-15C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.22-15C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.346-15C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.487-15C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.381-15C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.346-15C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.423-15C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.346-15C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.649-15C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.346-15C>G
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

19-6743191-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743191
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743191
    reference: chr 19
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.381-14T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.22-14T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.423-14T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.206-14T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.22-14T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.346-14T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.346-14T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.487-14T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.346-14T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.649-14T>C
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.346-14T>C
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-6743192-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743192
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743192
    reference: chr 19
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.346-13C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.22-13C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.649-13C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.423-13C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.381-13C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.206-13C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.346-13C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.346-13C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.22-13C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.487-13C>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.346-13C>G
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

19-6743192-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743192
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743192
    reference: chr 19
allele count: 3
allele frequency: 2.474757473767571e-5
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.649-13C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.346-13C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.487-13C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.423-13C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.22-13C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.346-13C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.346-13C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.206-13C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.346-13C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.381-13C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.22-13C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ

19-6743203-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743203
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743203
    reference: chr 19
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.649-2A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.206-2A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.346-2A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.22-2A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.346-2A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.346-2A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.487-2A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.22-2A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.381-2A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.346-2A>G
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.423-2A>G
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
hgvs: c.346-2A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-6743210-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743210
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743210
    reference: chr 19
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.428C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.351C>A
  hgvsp: ENSP00000472580.1:p.Phe117Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.27C>A
  hgvsp: ENSP00000471203.1:p.Phe9Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.211C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.351C>A
  hgvsp: ENSP00000320493.6:p.Phe117Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.351C>A
  hgvsp: ENSP00000320117.7:p.Phe117Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.492C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.351C>A
  hgvsp: ENSP00000469360.1:p.Phe117Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.27C>A
  hgvsp: ENSP00000471056.1:p.Phe9Leu
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.654C>A
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.386C>A
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe117Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

19-6743220-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743220
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 6743220
    reference: chr 19
allele count: 1
allele frequency: 8.26541913940456e-6
allele num: 120986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000596078
  gene symbol: TRIP10
  hgvsc: ENST00000596078.1:n.438C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320493
  ensembl transcript: ENST00000313285
  gene symbol: TRIP10
  hgvsc: ENST00000313285.8:c.361C>T
  hgvsp: ENSP00000320493.6:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000320117
  ensembl transcript: ENST00000313244
  gene symbol: TRIP10
  hgvsc: ENST00000313244.9:c.361C>T
  hgvsp: ENSP00000320117.7:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000469360
  ensembl transcript: ENST00000596758
  gene symbol: TRIP10
  hgvsc: ENST00000596758.1:c.361C>T
  hgvsp: ENSP00000469360.1:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471203
  ensembl transcript: ENST00000600428
  gene symbol: TRIP10
  hgvsc: ENST00000600428.1:c.37C>T
  hgvsp: ENSP00000471203.1:p.Arg13Trp
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000471056
  ensembl transcript: ENST00000596673
  gene symbol: TRIP10
  hgvsc: ENST00000596673.1:c.37C>T
  hgvsp: ENSP00000471056.1:p.Arg13Trp
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000125733
  ensembl protein: ENSP00000472580
  ensembl transcript: ENST00000600677
  gene symbol: TRIP10
  hgvsc: ENST00000600677.1:c.361C>T
  hgvsp: ENSP00000472580.1:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000600491
  gene symbol: TRIP10
  hgvsc: ENST00000600491.1:n.664C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000601303
  gene symbol: TRIP10
  hgvsc: ENST00000601303.1:n.221C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595305
  gene symbol: TRIP10
  hgvsc: ENST00000595305.1:n.396C>T
  variant of: http://identifiers.org/hgnc/12304
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000125733
  ensembl transcript: ENST00000595319
  gene symbol: TRIP10
  hgvsc: ENST00000595319.1:n.502C>T
  variant of: http://identifiers.org/hgnc/12304
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg121Trp
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

19-6743221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6743221
    reference: chr 19
allele count: 3
allele frequency: 2.480117722921248e-5
allele num: 120962
alternate allele: A
canonical: true
consequence: missense
filter: PASS
hgvs: p.Arg121Gln
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1929
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10728
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3099
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4052
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32975
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 190
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12326
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5076
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
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Other
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East 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: 0.0e0
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DP
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -9.599999999999999e-3

VQSLOD
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FS
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QD
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ReadPosRankSum
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SIO_000300: -1.159e0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Finnish)
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allele count: 4
allele frequency: 1.359619306594154e-3
allele num: 2942
num of homozygotes: 0

African
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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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European (Non-Finnish)
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allele frequency: 9.640437727983324e-4
allele num: 38380
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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MQRankSum
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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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ClippingRankSum
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ReadPosRankSum
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SIO_000300: 5.89e-1

BaseQRankSum
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SIO_000300: -7.05e-1

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: 3

East Asian
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allele frequency: 0.0e0
allele num: 3998
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 1920
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.004419445560466e-4
allele num: 29868
num of homozygotes: 0

South Asian
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ClippingRankSum
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SIO_000300: -1.77e-1

DP
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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FS
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SIO_000300: 1.153e0

BaseQRankSum
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SIO_000300: -8.84e-1

QD
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SIO_000300: 9.970000000000001e0

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: 0
allele frequency: 0.0e0
allele num: 5270
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 10482
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 frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 2.655337227827934e-4
allele num: 3766
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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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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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.13e1

MQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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FS
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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ClippingRankSum
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SIO_000300: 5.73e-1

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: 0
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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num of homozygotes: 0

European (Non-Finnish)
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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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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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BaseQRankSum
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SIO_000300: 8.76e-1

ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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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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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: 2
allele frequency: 8.943743851176102e-5
allele num: 22362
num of homozygotes: 0

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

Other
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European (Finnish)
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East Asian
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African
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South Asian
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European (Non-Finnish)
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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allele num: 10206
num of homozygotes: 0

East Asian
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European (Finnish)
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allele frequency: 3.024803387779795e-4
allele num: 6612
num of homozygotes: 0

Latino
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European (Non-Finnish)
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allele frequency: 3.336771218831523e-4
allele num: 65932
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.625446e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
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SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.503e1

GenotypeDepth
all individuals: 54
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.25e1
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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: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 882
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
allele num: 11560
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.516714190377965e-5
allele num: 65932
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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
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FS
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SIO_000300: 0.0e0

ReadPosRankSum
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MQ
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MQRankSum
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SIO_000300: 7.3e-2

ClippingRankSum
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SIO_000300: -2.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

QD
type: SiteQuality
SIO_000300: 1.503e1

DP
type: SiteQuality
SIO_000300: 1.625446e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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
type: Population
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: 4.547245884742474e-5
allele num: 65974
num of homozygotes: 0

African
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allele count: 0
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num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

MQ
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SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
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SIO_000300: 1.98e0

MQRankSum
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SIO_000300: -2.11e-1

VQSLOD
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SIO_000300: 1.07e0

ClippingRankSum
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SIO_000300: -5.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.6253e6

QD
type: SiteQuality
SIO_000300: 1.171e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1006
bin: 3.25e1
variant carriers: 0

African
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allele count: 1
allele frequency: 9.782821365681862e-5
allele num: 10222
num of homozygotes: 0

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

Latino
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
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66018
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15030
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 4.162e0

BaseQRankSum
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SIO_000300: -1.864e0

QD
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ReadPosRankSum
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SIO_000300: -9.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.97e-1

InbreedingCoeff
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SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.238e0

MQRankSum
type: SiteQuality
SIO_000300: -1.381e0

DP
type: SiteQuality
SIO_000300: 1.629994e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.320829480914014e-4
allele num: 15142
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66072
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.641404e6

QD
type: SiteQuality
SIO_000300: 1.289e1

FS
type: SiteQuality
SIO_000300: 4.524e0

InbreedingCoeff
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SIO_000300: -4.0e-4

BaseQRankSum
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MQRankSum
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 1.42e0

VQSLOD
type: SiteQuality
SIO_000300: 3.55e-1

ClippingRankSum
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SIO_000300: -3.48e-1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511076188461422e-5
allele num: 66178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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South Asian
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
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ReadPosRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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MQ
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QD
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MQRankSum
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SIO_000300: 2.04e0

DP
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GenotypeDepth
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variant carriers: 1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15462
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66218
num of homozygotes: 0

East Asian
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African
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allele count: 105
allele frequency: 1.021599532983071e-2
allele num: 10278
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Other
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-2

VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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DP
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MQRankSum
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FS
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 13
allele frequency: 1.123984091302092e-3
allele num: 11566
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 frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

European (Non-Finnish)
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allele num: 66218
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Other
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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allele frequency: 1.156604210039325e-4
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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

Latino
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allele frequency: 0.0e0
allele num: 11566
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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SIO_000300: 2.5e-2

MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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DP
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QD
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ReadPosRankSum
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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
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African
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Latino
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allele frequency: 1.729206294310911e-4
allele num: 11566
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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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ClippingRankSum
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DP
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QD
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MQ
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BaseQRankSum
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ReadPosRankSum
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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 count: 1
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allele num: 66244
num of homozygotes: 0

European (Finnish)
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African
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allele frequency: 2.917720287881735e-4
allele num: 10282
num of homozygotes: 0

Other
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Latino
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East Asian
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South Asian
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InbreedingCoeff
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FS
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MQRankSum
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DP
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ClippingRankSum
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QD
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BaseQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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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: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
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allele frequency: 2.913752913752914e-4
allele num: 10296
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66300
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Other
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QD
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SIO_000300: 1.289e1

MQRankSum
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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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FS
type: SiteQuality
SIO_000300: 6.33e-1

ReadPosRankSum
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SIO_000300: 7.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

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: 8648
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

African
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South Asian
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Other
type: Population
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 66434
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InbreedingCoeff
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QD
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FS
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

African
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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InbreedingCoeff
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ClippingRankSum
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DP
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ReadPosRankSum
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MQRankSum
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QD
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FS
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
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African
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European (Finnish)
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Latino
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Other
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East Asian
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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ReadPosRankSum
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DP
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ClippingRankSum
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QD
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BaseQRankSum
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VQSLOD
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

Latino
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allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.11e-1

FS
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SIO_000300: 3.901e0

MQRankSum
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QD
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DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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SIO_000300: 5.883e1

ReadPosRankSum
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SIO_000300: 1.66e0

BaseQRankSum
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SIO_000300: -8.59e-1

VQSLOD
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SIO_000300: -1.148e0

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 93

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8652
num of homozygotes: 0

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

Other
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allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

African
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allele count: 90
allele frequency: 8.665511265164644e-3
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 9.0e-2

FS
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SIO_000300: 2.437e0

InbreedingCoeff
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SIO_000300: 1.07e-2

BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 5.95e1

ClippingRankSum
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SIO_000300: 9.9e-2

DP
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SIO_000300: 1.691584e6

QD
type: SiteQuality
SIO_000300: 1.276e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

Latino
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allele frequency: 1.38264777048047e-3
allele num: 11572
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

European (Non-Finnish)
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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

South Asian
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QD
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SIO_000300: 1.173e1

MQ
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SIO_000300: 5.946e1

VQSLOD
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ClippingRankSum
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FS
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SIO_000300: 5.22e-1

DP
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ReadPosRankSum
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MQRankSum
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SIO_000300: -6.4e-2

BaseQRankSum
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SIO_000300: -1.126e0

InbreedingCoeff
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SIO_000300: -2.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997961386257345e-5
allele num: 66712
num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
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SIO_000300: 2.91e-2

BaseQRankSum
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SIO_000300: 8.54e-1

ReadPosRankSum
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ClippingRankSum
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SIO_000300: -3.17e-1

QD
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VQSLOD
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MQRankSum
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FS
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.682526e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

Other
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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 (Non-Finnish)
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allele num: 66728
num of homozygotes: 0

African
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num of homozygotes: 0

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

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: 8.25e1
variant carriers: 0

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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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66728
num of homozygotes: 0

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

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: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
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allele num: 66726
num of homozygotes: 0

South Asian
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allele num: 16512
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Latino
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African
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Other
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European (Finnish)
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East Asian
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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MQ
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QD
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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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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African
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South Asian
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Latino
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European (Finnish)
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Other
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East Asian
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VQSLOD
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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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ReadPosRankSum
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MQRankSum
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MQ
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ClippingRankSum
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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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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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InbreedingCoeff
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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FS
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VQSLOD
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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African
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Other
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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QD
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FS
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ReadPosRankSum
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MQ
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DP
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MQRankSum
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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
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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Latino
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DP
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10400
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Other
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South Asian
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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FS
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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DP
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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DP
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FS
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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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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European (Finnish)
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Latino
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East Asian
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African
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South Asian
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European (Non-Finnish)
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QD
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MQRankSum
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MQ
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

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

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

East Asian
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allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.08e-1

ReadPosRankSum
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SIO_000300: 5.16e-1

FS
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SIO_000300: 7.862e0

BaseQRankSum
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SIO_000300: 5.45e0

QD
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SIO_000300: 1.586e1

MQ
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SIO_000300: 5.728e1

MQRankSum
type: SiteQuality
SIO_000300: -8.46e-1

DP
type: SiteQuality
SIO_000300: 1.682713e6

VQSLOD
type: SiteQuality
SIO_000300: -1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
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 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: 11572
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
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SIO_000300: -5.242e-1

QD
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -5.824e0

FS
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SIO_000300: 4.152e0

InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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SIO_000300: -2.104e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

DP
type: SiteQuality
SIO_000300: 1.682556e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

East Asian
type: Population
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
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.178e0

ReadPosRankSum
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SIO_000300: -2.557e0

InbreedingCoeff
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SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 3.814e0

BaseQRankSum
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SIO_000300: -2.13e-1

MQRankSum
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.682115e6

MQ
type: SiteQuality
SIO_000300: 5.932e1

QD
type: SiteQuality
SIO_000300: 8.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 482
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GenotypeQuality
all individuals: 2684
bin: 7.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.004e0

DP
type: SiteQuality
SIO_000300: 1.681107e6

BaseQRankSum
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SIO_000300: 4.49e0

QD
type: SiteQuality
SIO_000300: 1.293e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.409999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2682
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GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-2

BaseQRankSum
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DP
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VQSLOD
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
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SIO_000300: 1.247e0

QD
type: SiteQuality
SIO_000300: 1.411e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-2

GenotypeDepth
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variant carriers: 0

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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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

BaseQRankSum
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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DP
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
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MQRankSum
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ReadPosRankSum
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FS
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.49940004799616e-5
allele num: 66672
num of homozygotes: 0

VQSLOD
type: SiteQuality
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FS
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.76e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

DP
type: SiteQuality
SIO_000300: 1.674164e6

GenotypeQuality
all individuals: 460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1828
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.402e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.42e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 1.673327e6

MQRankSum
type: SiteQuality
SIO_000300: 4.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.38e-1

FS
type: SiteQuality
SIO_000300: 6.513e0

VQSLOD
type: SiteQuality
SIO_000300: 7.48e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

GenotypeQuality
all individuals: 2526
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.227e1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.38e-1

DP
type: SiteQuality
SIO_000300: 1.673327e6

MQRankSum
type: SiteQuality
SIO_000300: 4.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.42e-1

FS
type: SiteQuality
SIO_000300: 6.513e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.402e0

VQSLOD
type: SiteQuality
SIO_000300: 7.48e-1

GenotypeQuality
all individuals: 120
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 134
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variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41626
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1822
bin: 9.75e1
variant carriers: 1

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.569e1

MQRankSum
type: SiteQuality
SIO_000300: -1.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.399999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.229e0

FS
type: SiteQuality
SIO_000300: 4.777e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e0

DP
type: SiteQuality
SIO_000300: 1.671736e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 154
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 129
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variant carriers: 0

GenotypeQuality
all individuals: 231
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 149
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GenotypeQuality
all individuals: 8721
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 102
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1808
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variant carriers: 1

GenotypeQuality
all individuals: 2602
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

QD
type: SiteQuality
SIO_000300: 1.482e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.670687e6

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
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variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 167
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1807
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.492e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.059e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.04e-1

FS
type: SiteQuality
SIO_000300: 6.739e0

VQSLOD
type: SiteQuality
SIO_000300: 6.2e-1

DP
type: SiteQuality
SIO_000300: 1.669514e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
all individuals: 141
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2593
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variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499640028797696e-5
allele num: 66672
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.357e1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 4.42e-1

DP
type: SiteQuality
SIO_000300: 1.667484e6

GenotypeQuality
all individuals: 2470
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 184
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GenotypeQuality
all individuals: 415
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GenotypeQuality
all individuals: 443
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variant carriers: 0

GenotypeQuality
all individuals: 8709
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.66652e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.88e1

MQRankSum
type: SiteQuality
SIO_000300: 4.99e-1

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

VQSLOD
type: SiteQuality
SIO_000300: -4.821e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 162
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GenotypeQuality
all individuals: 1791
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

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

VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -2.218e0

InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.665992e6

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

QD
type: SiteQuality
SIO_000300: 1.128e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
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African
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allele count: 0
allele frequency: 0.0e0
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MQ
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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VQSLOD
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InbreedingCoeff
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DP
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SIO_000300: 1.665372e6

MQRankSum
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SIO_000300: -4.7e-2

QD
type: SiteQuality
SIO_000300: 1.496e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 8
allele frequency: 1.199868014518403e-4
allele num: 66674
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
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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allele frequency: 0.0e0
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FS
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DP
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VQSLOD
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QD
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MQRankSum
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SIO_000300: 8.129999999999999e-1

ClippingRankSum
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InbreedingCoeff
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SIO_000300: 1.1e-3

BaseQRankSum
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SIO_000300: -2.946e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.38e-1

VQSLOD
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SIO_000300: -3.272e0

ClippingRankSum
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SIO_000300: -2.969e0

FS
type: SiteQuality
SIO_000300: 5.471e0

QD
type: SiteQuality
SIO_000300: 1.349e1

MQ
type: SiteQuality
SIO_000300: 5.823e1

DP
type: SiteQuality
SIO_000300: 1.661422e6

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-2

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16504
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VQSLOD
type: SiteQuality
SIO_000300: -5.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.67e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.256e0

FS
type: SiteQuality
SIO_000300: 2.046e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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ClippingRankSum
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SIO_000300: 1.25e0

QD
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SIO_000300: 1.068e1

DP
type: SiteQuality
SIO_000300: 1.661524e6

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.98e-1

DP
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MQRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.4861e1

BaseQRankSum
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SIO_000300: -3.91e-1

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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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

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

Latino
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allele count: 2
allele frequency: 1.729804532087874e-4
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

European (Finnish)
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allele count: 0
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Other
type: Population
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DP
type: SiteQuality
SIO_000300: 1.661337e6

MQRankSum
type: SiteQuality
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VQSLOD
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MQ
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 5.21e-1

BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

Other
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South Asian
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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
allele num: 11562
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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
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FS
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MQ
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QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
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SIO_000300: 3.21e-1

QD
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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MQ
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DP
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VQSLOD
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ClippingRankSum
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SIO_000300: 2.2e-2

FS
type: SiteQuality
SIO_000300: 2.1261e1

MQRankSum
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SIO_000300: -3.059e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 66654
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
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African
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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

Other
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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: 1
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allele num: 16510
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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DP
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FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: -4.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.51e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
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 count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

FS
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MQRankSum
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QD
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DP
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MQ
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VQSLOD
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ClippingRankSum
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SIO_000300: 9.11e-1

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: 3.49e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

South 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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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ReadPosRankSum
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SIO_000300: 7.000000000000001e-2

InbreedingCoeff
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SIO_000300: 2.0e-4

FS
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SIO_000300: 0.0e0

MQRankSum
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BaseQRankSum
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QD
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SIO_000300: 1.383e1

DP
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

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

African
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allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

East Asian
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allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 904
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European (Non-Finnish)
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allele frequency: 1.500240038406145e-5
allele num: 66656
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

South Asian
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allele num: 16504
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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InbreedingCoeff
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FS
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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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European (Non-Finnish)
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allele num: 66602
num of homozygotes: 0

Latino
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European (Finnish)
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South Asian
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East Asian
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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MQRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
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num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502403846153846e-5
allele num: 66560
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 6.238e0

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 1.655837e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

QD
type: SiteQuality
SIO_000300: 1.23e1