10-97096980-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97096980
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97096980
    reference: chr 10
allele count: 8
allele frequency: 7.481529972879454e-5
allele num: 106930
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2937C>G
  hgvsp: ENST00000371247.2:c.2937C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2799C>G
  hgvsp: ENST00000371227.4:c.2799C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-418C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1910C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1910C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1910C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1910C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1910C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2937C>G
  hgvsp: ENST00000361941.3:c.2937C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1910C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1910C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1910C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1910C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1910C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-418C>G
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro979Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

10-97096982-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97096982
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97096982
    reference: chr 10
allele count: 1
allele frequency: 9.359264736162327e-6
allele num: 106846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1908C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-420C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1908C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-420C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1908C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1908C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1908C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1908C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1908C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2935C>T
  hgvsp: ENSP00000355136.3:p.Pro979Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2797C>T
  hgvsp: ENSP00000360271.3:p.Pro933Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2935C>T
  hgvsp: ENSP00000360293.2:p.Pro979Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1908C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1908C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1908C>T
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro979Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

10-97096983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97096983
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97096983
    reference: chr 10
allele count: 1
allele frequency: 9.390905846777981e-6
allele num: 106486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1907C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1907C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1907C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1907C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2934C>T
  hgvsp: ENST00000361941.3:c.2934C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1907C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-421C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1907C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-421C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2934C>T
  hgvsp: ENST00000371247.2:c.2934C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1907C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1907C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1907C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2796C>T
  hgvsp: ENST00000371227.4:c.2796C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1907C>T
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14190
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser978Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-97096983-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97096983
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97096983
    reference: chr 10
allele count: 1
allele frequency: 9.390905846777981e-6
allele num: 106486
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-421C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1907C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1907C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2934C>A
  hgvsp: ENST00000371247.2:c.2934C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1907C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1907C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1907C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1907C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1907C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2796C>A
  hgvsp: ENST00000371227.4:c.2796C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-421C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2934C>A
  hgvsp: ENST00000361941.3:c.2934C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1907C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1907C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1907C>A
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser978Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

10-97096990-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97096990
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97096990
    reference: chr 10
allele count: 1
allele frequency: 9.728383531792358e-6
allele num: 102792
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2927C>T
  hgvsp: ENSP00000360293.2:p.Ala976Val
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1900C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2927C>T
  hgvsp: ENSP00000355136.3:p.Ala976Val
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1900C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1900C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2789C>T
  hgvsp: ENSP00000360271.3:p.Ala930Val
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-428C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1900C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1900C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1900C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1900C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-428C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1900C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1900C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1900C>T
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala976Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS

10-97096990-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97096990
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97096990
    reference: chr 10
allele count: 1
allele frequency: 9.728383531792358e-6
allele num: 102792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1900C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-428C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2789C>A
  hgvsp: ENSP00000360271.3:p.Ala930Asp
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1900C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1900C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1900C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1900C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1900C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2927C>A
  hgvsp: ENSP00000360293.2:p.Ala976Asp
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2927C>A
  hgvsp: ENSP00000355136.3:p.Ala976Asp
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-428C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1900C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1900C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1900C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1900C>A
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala976Asp
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

10-97096993-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97096993
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97096993
    reference: chr 10
allele count: 8
allele frequency: 7.859935941522077e-5
allele num: 101782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1897G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2924G>A
  hgvsp: ENSP00000360293.2:p.Arg975Gln
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1897G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2924G>A
  hgvsp: ENSP00000355136.3:p.Arg975Gln
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1897G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2786G>A
  hgvsp: ENSP00000360271.3:p.Arg929Gln
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1897G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1897G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-431G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1897G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1897G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1897G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1897G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-431G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1897G>A
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6963
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg975Gln
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

10-97096994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97096994
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97096994
    reference: chr 10
allele count: 4
allele frequency: 3.954913980620922e-5
allele num: 101140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1896C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1896C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1896C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1896C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1896C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-432C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2923C>T
  hgvsp: ENSP00000360293.2:p.Arg975Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-432C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2923C>T
  hgvsp: ENSP00000355136.3:p.Arg975Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1896C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1896C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1896C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2785C>T
  hgvsp: ENSP00000360271.3:p.Arg929Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1896C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1896C>T
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg975Ter
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

10-97096996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97096996
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97096996
    reference: chr 10
allele count: 11
allele frequency: 1.089626753308503e-4
allele num: 100952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-434G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1894G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2783G>A
  hgvsp: ENSP00000360271.3:p.Arg928His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2921G>A
  hgvsp: ENSP00000360293.2:p.Arg974His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1894G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1894G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1894G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1894G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1894G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1894G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2921G>A
  hgvsp: ENSP00000355136.3:p.Arg974His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1894G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-434G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1894G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1894G>A
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg974His
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

10-97096997-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97096997
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97096997
    reference: chr 10
allele count: 4
allele frequency: 3.97748742119603e-5
allele num: 100566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1893C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1893C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2920C>T
  hgvsp: ENSP00000355136.3:p.Arg974Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1893C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-435C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2782C>T
  hgvsp: ENSP00000360271.3:p.Arg928Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1893C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1893C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1893C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2920C>T
  hgvsp: ENSP00000360293.2:p.Arg974Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1893C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1893C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1893C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1893C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-435C>T
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg974Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

10-97097003-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97097003
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97097003
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 99024
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2776C>G
  hgvsp: ENSP00000360271.3:p.His926Asp
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1887C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1887C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-441C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2914C>G
  hgvsp: ENSP00000360293.2:p.His972Asp
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-441C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1887C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1887C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1887C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2914C>G
  hgvsp: ENSP00000355136.3:p.His972Asp
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1887C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1887C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1887C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1887C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1887C>G
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8052
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His972Asp
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

10-97097005-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97097005
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97097005
    reference: chr 10
allele count: 1
allele frequency: 1.014981121351143e-5
allele num: 98524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2912C>A
  hgvsp: ENSP00000355136.3:p.Pro971His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1885C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1885C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-443C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1885C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2774C>A
  hgvsp: ENSP00000360271.3:p.Pro925His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1885C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1885C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2912C>A
  hgvsp: ENSP00000360293.2:p.Pro971His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1885C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1885C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1885C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1885C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1885C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-443C>A
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro971His
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

10-97097016-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97097016
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97097016
    reference: chr 10
allele count: 1
allele frequency: 1.070916061599092e-5
allele num: 93378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2901C>G
  hgvsp: ENST00000361941.3:c.2901C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1874C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1874C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1874C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1874C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1874C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-454C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2901C>G
  hgvsp: ENST00000371247.2:c.2901C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1874C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2763C>G
  hgvsp: ENST00000371227.4:c.2763C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1874C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-454C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1874C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1874C>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1874C>G
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10657
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro967Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

10-97097017-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97097017
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97097017
    reference: chr 10
allele count: 1
allele frequency: 1.070457513541288e-5
allele num: 93418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1873C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1873C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1873C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1873C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2900C>A
  hgvsp: ENSP00000360293.2:p.Pro967His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1873C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1873C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1873C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-455C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2762C>A
  hgvsp: ENSP00000360271.3:p.Pro921His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1873C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2900C>A
  hgvsp: ENSP00000355136.3:p.Pro967His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-455C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1873C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1873C>A
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8941
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10013
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro967His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

10-97097026-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97097026
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97097026
    reference: chr 10
allele count: 26
allele frequency: 2.926411993787002e-4
allele num: 88846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2753C>T
  hgvsp: ENSP00000360271.3:p.Thr918Met
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2891C>T
  hgvsp: ENSP00000360293.2:p.Thr964Met
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-464C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1864C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2891C>T
  hgvsp: ENSP00000355136.3:p.Thr964Met
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1864C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1864C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1864C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1864C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1864C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1864C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-464C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1864C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1864C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1864C>T
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 10952
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20237
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Thr964Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

10-97097054-TAAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97097054
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97097050
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 59772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1832_2418+1835delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1832_2775+1835delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1832_2196+1835delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1832_1815+1835delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2728-7_2728-4delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1832_2211+1835delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1832_2106+1835delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1832_2301+1835delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2866-7_2866-4delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1832_3645+1835delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-496_2932-493delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2866-7_2866-4delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1832_2418+1835delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1832_2775+1835delTTTT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-496_2932-493delTTTT
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19737
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21194
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2866-7_2866-4delTTTT
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: TAAAA
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

10-97097064-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97097064
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97097064
    reference: chr 10
allele count: 3
allele frequency: 7.145579268292682e-5
allele num: 41984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1826T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1826T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1826T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1826T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1826T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1826T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-502T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1826T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1826T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1826T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2866-13T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2866-13T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2728-13T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-502T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1826T>C
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14023
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-97097094-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97097094
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97097094
    reference: chr 10
allele count: 1
allele frequency: 5.159426271798576e-5
allele num: 19382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1796T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-532T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1796T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1796T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1796T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1796T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1796T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-532T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1796T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1796T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2728-43T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1796T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1796T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2866-43T>C
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2866-43T>C
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8152
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD

10-97097096-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97097096
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97097096
    reference: chr 10
allele count: 1
allele frequency: 5.435964340073929e-5
allele num: 18396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1794C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1794C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-534C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1794C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1794C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1794C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1794C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2866-45C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1794C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1794C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1794C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2728-45C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2866-45C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1794C>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-534C>A
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/10-97097100-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97097100
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97097100
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 15786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2932-538G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+1790G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+1790G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2866-49G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2932-538G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+1790G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+1790G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+1790G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+1790G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2728-49G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+1790G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+1790G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+1790G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+1790G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2866-49G>T
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 20897
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6999
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

10-97098840-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098840
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098840
    reference: chr 10
allele count: 3
allele frequency: 2.682259535432648e-5
allele num: 111846
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2865+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2931+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2727+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2931+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+50G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2865+50G>A
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/10-97098850-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098850
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098849
    reference: chr 10
allele count: 5
allele frequency: 4.468195385247806e-5
allele num: 111902
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2865+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2727+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2931+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2931+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2865+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+39delT
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+39delT
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: CA
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

10-97098859-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098859
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098859
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 112100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2931+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2865+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2727+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2865+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2931+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+31A>G
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+31A>G
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/10-97098874-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098874
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098874
    reference: chr 10
allele count: 1
allele frequency: 8.880994671403197e-6
allele num: 112600
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2865+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2727+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2931+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2931+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2865+16G>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+16G>T
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

10-97098874-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098874
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098874
    reference: chr 10
allele count: 10
allele frequency: 8.880994671403197e-5
allele num: 112600
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2931+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2865+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2727+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2931+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2865+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+16G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+16G>A
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

10-97098875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098875
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098875
    reference: chr 10
allele count: 5
allele frequency: 4.429090264859598e-5
allele num: 112890
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2865+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2931+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2727+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2865+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2931+15C>T
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+15C>T
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

10-97098881-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098881
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098881
    reference: chr 10
allele count: 2
allele frequency: 1.765536723163842e-5
allele num: 113280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2775+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2301+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2211+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2865+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2106+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1815+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3645+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2196+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2418+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2418+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2931+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2931+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2865+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2727+9G>A
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2775+9G>A
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum

10-97098892-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098892
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098892
    reference: chr 10
allele count: 1
allele frequency: 8.747222756774724e-6
allele num: 114322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2929C>T
  hgvsp: ENSP00000360292.2:p.Gln977Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2416C>T
  hgvsp: ENSP00000360291.2:p.Gln806Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3643C>T
  hgvsp: ENSP00000475901.1:p.Gln1215Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2863C>T
  hgvsp: ENSP00000355136.3:p.Gln955Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2104C>T
  hgvsp: ENSP00000302556.6:p.Gln702Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2725C>T
  hgvsp: ENSP00000360271.3:p.Gln909Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2416C>T
  hgvsp: ENSP00000343998.5:p.Gln806Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2194C>T
  hgvsp: ENSP00000360283.1:p.Gln732Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2863C>T
  hgvsp: ENSP00000360293.2:p.Gln955Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2299C>T
  hgvsp: ENSP00000277985.5:p.Gln767Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1813C>T
  hgvsp: ENSP00000360285.1:p.Gln605Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2929C>T
  hgvsp: ENSP00000277982.5:p.Gln977Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2773C>T
  hgvsp: ENSP00000377521.1:p.Gln925Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2773C>T
  hgvsp: ENSP00000277984.4:p.Gln925Ter
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2209C>T
  hgvsp: ENSP00000360295.2:p.Gln737Ter
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln955Ter
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

10-97098897-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098897
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098897
    reference: chr 10
allele count: 2
allele frequency: 1.744044089434581e-5
allele num: 114676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2924G>A
  hgvsp: ENSP00000277982.5:p.Ser975Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2411G>A
  hgvsp: ENSP00000360291.2:p.Ser804Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2411G>A
  hgvsp: ENSP00000343998.5:p.Ser804Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2924G>A
  hgvsp: ENSP00000360292.2:p.Ser975Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2294G>A
  hgvsp: ENSP00000277985.5:p.Ser765Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2768G>A
  hgvsp: ENSP00000377521.1:p.Ser923Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2099G>A
  hgvsp: ENSP00000302556.6:p.Ser700Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2189G>A
  hgvsp: ENSP00000360283.1:p.Ser730Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2858G>A
  hgvsp: ENSP00000360293.2:p.Ser953Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2720G>A
  hgvsp: ENSP00000360271.3:p.Ser907Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1808G>A
  hgvsp: ENSP00000360285.1:p.Ser603Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2204G>A
  hgvsp: ENSP00000360295.2:p.Ser735Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2768G>A
  hgvsp: ENSP00000277984.4:p.Ser923Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3638G>A
  hgvsp: ENSP00000475901.1:p.Ser1213Asn
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2858G>A
  hgvsp: ENSP00000355136.3:p.Ser953Asn
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9263
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser953Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

10-97098912-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098912
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098912
    reference: chr 10
allele count: 2
allele frequency: 1.71609006040637e-5
allele num: 116544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2753G>A
  hgvsp: ENSP00000377521.1:p.Arg918His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2909G>A
  hgvsp: ENSP00000360292.2:p.Arg970His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3623G>A
  hgvsp: ENSP00000475901.1:p.Arg1208His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2843G>A
  hgvsp: ENSP00000355136.3:p.Arg948His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2279G>A
  hgvsp: ENSP00000277985.5:p.Arg760His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2396G>A
  hgvsp: ENSP00000343998.5:p.Arg799His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2084G>A
  hgvsp: ENSP00000302556.6:p.Arg695His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2909G>A
  hgvsp: ENSP00000277982.5:p.Arg970His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2189G>A
  hgvsp: ENSP00000360295.2:p.Arg730His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2705G>A
  hgvsp: ENSP00000360271.3:p.Arg902His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2843G>A
  hgvsp: ENSP00000360293.2:p.Arg948His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2396G>A
  hgvsp: ENSP00000360291.2:p.Arg799His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2753G>A
  hgvsp: ENSP00000277984.4:p.Arg918His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2174G>A
  hgvsp: ENSP00000360283.1:p.Arg725His
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1793G>A
  hgvsp: ENSP00000360285.1:p.Arg598His
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg948His
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

10-97098913-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098913
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098913
    reference: chr 10
allele count: 1
allele frequency: 8.542627712284299e-6
allele num: 117060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2908C>T
  hgvsp: ENSP00000360292.2:p.Arg970Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2908C>T
  hgvsp: ENSP00000277982.5:p.Arg970Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2842C>T
  hgvsp: ENSP00000355136.3:p.Arg948Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2188C>T
  hgvsp: ENSP00000360295.2:p.Arg730Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2842C>T
  hgvsp: ENSP00000360293.2:p.Arg948Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3622C>T
  hgvsp: ENSP00000475901.1:p.Arg1208Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2395C>T
  hgvsp: ENSP00000360291.2:p.Arg799Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2752C>T
  hgvsp: ENSP00000377521.1:p.Arg918Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2083C>T
  hgvsp: ENSP00000302556.6:p.Arg695Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1792C>T
  hgvsp: ENSP00000360285.1:p.Arg598Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2278C>T
  hgvsp: ENSP00000277985.5:p.Arg760Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2704C>T
  hgvsp: ENSP00000360271.3:p.Arg902Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2395C>T
  hgvsp: ENSP00000343998.5:p.Arg799Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2173C>T
  hgvsp: ENSP00000360283.1:p.Arg725Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2752C>T
  hgvsp: ENSP00000277984.4:p.Arg918Cys
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg948Cys
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/10-97098915-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098915
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098915
    reference: chr 10
allele count: 3
allele frequency: 2.557108762359359e-5
allele num: 117320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2750G>T
  hgvsp: ENSP00000277984.4:p.Ser917Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2906G>T
  hgvsp: ENSP00000360292.2:p.Ser969Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2186G>T
  hgvsp: ENSP00000360295.2:p.Ser729Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3620G>T
  hgvsp: ENSP00000475901.1:p.Ser1207Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2276G>T
  hgvsp: ENSP00000277985.5:p.Ser759Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2393G>T
  hgvsp: ENSP00000343998.5:p.Ser798Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2702G>T
  hgvsp: ENSP00000360271.3:p.Ser901Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2393G>T
  hgvsp: ENSP00000360291.2:p.Ser798Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1790G>T
  hgvsp: ENSP00000360285.1:p.Ser597Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2750G>T
  hgvsp: ENSP00000377521.1:p.Ser917Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2840G>T
  hgvsp: ENSP00000360293.2:p.Ser947Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2171G>T
  hgvsp: ENSP00000360283.1:p.Ser724Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2081G>T
  hgvsp: ENSP00000302556.6:p.Ser694Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2840G>T
  hgvsp: ENSP00000355136.3:p.Ser947Ile
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2906G>T
  hgvsp: ENSP00000277982.5:p.Ser969Ile
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser947Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-97098918-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098918
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098918
    reference: chr 10
allele count: 90
allele frequency: 7.637215301585146e-4
allele num: 117844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2390C>T
  hgvsp: ENSP00000360291.2:p.Pro797Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2078C>T
  hgvsp: ENSP00000302556.6:p.Pro693Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2168C>T
  hgvsp: ENSP00000360283.1:p.Pro723Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3617C>T
  hgvsp: ENSP00000475901.1:p.Pro1206Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2390C>T
  hgvsp: ENSP00000343998.5:p.Pro797Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2747C>T
  hgvsp: ENSP00000377521.1:p.Pro916Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2837C>T
  hgvsp: ENSP00000360293.2:p.Pro946Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2903C>T
  hgvsp: ENSP00000277982.5:p.Pro968Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2837C>T
  hgvsp: ENSP00000355136.3:p.Pro946Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2903C>T
  hgvsp: ENSP00000360292.2:p.Pro968Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1787C>T
  hgvsp: ENSP00000360285.1:p.Pro596Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2273C>T
  hgvsp: ENSP00000277985.5:p.Pro758Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2699C>T
  hgvsp: ENSP00000360271.3:p.Pro900Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2183C>T
  hgvsp: ENSP00000360295.2:p.Pro728Leu
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2747C>T
  hgvsp: ENSP00000277984.4:p.Pro916Leu
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10434
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 9.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro946Leu
num of homozygotes: 1
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

10-97098919-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098919
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098919
    reference: chr 10
allele count: 1
allele frequency: 8.4774499830451e-6
allele num: 117960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2746C>T
  hgvsp: ENSP00000277984.4:p.Pro916Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2836C>T
  hgvsp: ENSP00000355136.3:p.Pro946Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2182C>T
  hgvsp: ENSP00000360295.2:p.Pro728Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2167C>T
  hgvsp: ENSP00000360283.1:p.Pro723Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2698C>T
  hgvsp: ENSP00000360271.3:p.Pro900Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2836C>T
  hgvsp: ENSP00000360293.2:p.Pro946Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2389C>T
  hgvsp: ENSP00000343998.5:p.Pro797Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2389C>T
  hgvsp: ENSP00000360291.2:p.Pro797Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2902C>T
  hgvsp: ENSP00000277982.5:p.Pro968Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3616C>T
  hgvsp: ENSP00000475901.1:p.Pro1206Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1786C>T
  hgvsp: ENSP00000360285.1:p.Pro596Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2746C>T
  hgvsp: ENSP00000377521.1:p.Pro916Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2272C>T
  hgvsp: ENSP00000277985.5:p.Pro758Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2902C>T
  hgvsp: ENSP00000360292.2:p.Pro968Ser
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2077C>T
  hgvsp: ENSP00000302556.6:p.Pro693Ser
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro946Ser
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

10-97098919-GGGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098919
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098916
    reference: chr 10
allele count: 3
allele frequency: 2.54323499491353e-5
allele num: 117960
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2743_2745delTCC
  hgvsp: ENSP00000277984.4:p.Ser915del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3613_3615delTCC
  hgvsp: ENSP00000475901.1:p.Ser1205del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1783_1785delTCC
  hgvsp: ENSP00000360285.1:p.Ser595del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2386_2388delTCC
  hgvsp: ENSP00000360291.2:p.Ser796del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2179_2181delTCC
  hgvsp: ENSP00000360295.2:p.Ser727del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2164_2166delTCC
  hgvsp: ENSP00000360283.1:p.Ser722del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2743_2745delTCC
  hgvsp: ENSP00000377521.1:p.Ser915del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2899_2901delTCC
  hgvsp: ENSP00000277982.5:p.Ser967del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2386_2388delTCC
  hgvsp: ENSP00000343998.5:p.Ser796del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2074_2076delTCC
  hgvsp: ENSP00000302556.6:p.Ser692del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2269_2271delTCC
  hgvsp: ENSP00000277985.5:p.Ser757del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2695_2697delTCC
  hgvsp: ENSP00000360271.3:p.Ser899del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2899_2901delTCC
  hgvsp: ENSP00000360292.2:p.Ser967del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2833_2835delTCC
  hgvsp: ENSP00000360293.2:p.Ser945del
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2833_2835delTCC
  hgvsp: ENSP00000355136.3:p.Ser945del
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser945del
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: GGGA
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

10-97098920-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098920
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098920
    reference: chr 10
allele count: 1
allele frequency: 8.468547813420954e-6
allele num: 118084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2388C>T
  hgvsp: ENST00000353505.5:c.2388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2745C>T
  hgvsp: ENST00000354106.3:c.2745C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2835C>T
  hgvsp: ENST00000371247.2:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2745C>T
  hgvsp: ENST00000393949.1:c.2745C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2388C>T
  hgvsp: ENST00000371245.3:c.2388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2181C>T
  hgvsp: ENST00000371249.2:c.2181C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2271C>T
  hgvsp: ENST00000347291.4:c.2271C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2166C>T
  hgvsp: ENST00000371239.1:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2901C>T
  hgvsp: ENST00000371246.2:c.2901C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2835C>T
  hgvsp: ENST00000361941.3:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1785C>T
  hgvsp: ENST00000371241.1:c.1785C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2697C>T
  hgvsp: ENST00000371227.4:c.2697C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3615C>T
  hgvsp: ENST00000607232.1:c.3615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2076C>T
  hgvsp: ENST00000306402.6:c.2076C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2901C>T
  hgvsp: ENST00000277982.5:c.2901C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser945Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

10-97098921-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098921
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098921
    reference: chr 10
allele count: 1
allele frequency: 8.459091831900928e-6
allele num: 118216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2387C>G
  hgvsp: ENSP00000343998.5:p.Ser796Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2834C>G
  hgvsp: ENSP00000360293.2:p.Ser945Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2075C>G
  hgvsp: ENSP00000302556.6:p.Ser692Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2900C>G
  hgvsp: ENSP00000277982.5:p.Ser967Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2744C>G
  hgvsp: ENSP00000277984.4:p.Ser915Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2900C>G
  hgvsp: ENSP00000360292.2:p.Ser967Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2180C>G
  hgvsp: ENSP00000360295.2:p.Ser727Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2744C>G
  hgvsp: ENSP00000377521.1:p.Ser915Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2270C>G
  hgvsp: ENSP00000277985.5:p.Ser757Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2834C>G
  hgvsp: ENSP00000355136.3:p.Ser945Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2387C>G
  hgvsp: ENSP00000360291.2:p.Ser796Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2696C>G
  hgvsp: ENSP00000360271.3:p.Ser899Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3614C>G
  hgvsp: ENSP00000475901.1:p.Ser1205Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2165C>G
  hgvsp: ENSP00000360283.1:p.Ser722Cys
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1784C>G
  hgvsp: ENSP00000360285.1:p.Ser595Cys
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser945Cys
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

10-97098939-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098939
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098939
    reference: chr 10
allele count: 1
allele frequency: 8.320852055250457e-6
allele num: 120180
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2147A>G
  hgvsp: ENSP00000360283.1:p.Asp716Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2057A>G
  hgvsp: ENSP00000302556.6:p.Asp686Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2816A>G
  hgvsp: ENSP00000360293.2:p.Asp939Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2882A>G
  hgvsp: ENSP00000360292.2:p.Asp961Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2369A>G
  hgvsp: ENSP00000343998.5:p.Asp790Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2162A>G
  hgvsp: ENSP00000360295.2:p.Asp721Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2726A>G
  hgvsp: ENSP00000277984.4:p.Asp909Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1766A>G
  hgvsp: ENSP00000360285.1:p.Asp589Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2882A>G
  hgvsp: ENSP00000277982.5:p.Asp961Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2369A>G
  hgvsp: ENSP00000360291.2:p.Asp790Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3596A>G
  hgvsp: ENSP00000475901.1:p.Asp1199Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2726A>G
  hgvsp: ENSP00000377521.1:p.Asp909Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2816A>G
  hgvsp: ENSP00000355136.3:p.Asp939Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2252A>G
  hgvsp: ENSP00000277985.5:p.Asp751Gly
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2678A>G
  hgvsp: ENSP00000360271.3:p.Asp893Gly
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp939Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

10-97098942-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97098942
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97098942
    reference: chr 10
allele count: 5
allele frequency: 4.151237899141524e-5
allele num: 120446
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277984
  ensembl transcript: ENST00000354106
  gene symbol: SORBS1
  hgvsc: ENST00000354106.3:c.2723T>C
  hgvsp: ENSP00000277984.4:p.Met908Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000302556
  ensembl transcript: ENST00000306402
  gene symbol: SORBS1
  hgvsc: ENST00000306402.6:c.2054T>C
  hgvsp: ENSP00000302556.6:p.Met685Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000355136
  ensembl transcript: ENST00000361941
  gene symbol: SORBS1
  hgvsc: ENST00000361941.3:c.2813T>C
  hgvsp: ENSP00000355136.3:p.Met938Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360283
  ensembl transcript: ENST00000371239
  gene symbol: SORBS1
  hgvsc: ENST00000371239.1:c.2144T>C
  hgvsp: ENSP00000360283.1:p.Met715Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277982
  ensembl transcript: ENST00000277982
  gene symbol: SORBS1
  hgvsc: ENST00000277982.5:c.2879T>C
  hgvsp: ENSP00000277982.5:p.Met960Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000377521
  ensembl transcript: ENST00000393949
  gene symbol: SORBS1
  hgvsc: ENST00000393949.1:c.2723T>C
  hgvsp: ENSP00000377521.1:p.Met908Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000475901
  ensembl transcript: ENST00000607232
  gene symbol: SORBS1
  hgvsc: ENST00000607232.1:c.3593T>C
  hgvsp: ENSP00000475901.1:p.Met1198Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360285
  ensembl transcript: ENST00000371241
  gene symbol: SORBS1
  hgvsc: ENST00000371241.1:c.1763T>C
  hgvsp: ENSP00000360285.1:p.Met588Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360293
  ensembl transcript: ENST00000371247
  gene symbol: SORBS1
  hgvsc: ENST00000371247.2:c.2813T>C
  hgvsp: ENSP00000360293.2:p.Met938Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360292
  ensembl transcript: ENST00000371246
  gene symbol: SORBS1
  hgvsc: ENST00000371246.2:c.2879T>C
  hgvsp: ENSP00000360292.2:p.Met960Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000277985
  ensembl transcript: ENST00000347291
  gene symbol: SORBS1
  hgvsc: ENST00000347291.4:c.2249T>C
  hgvsp: ENSP00000277985.5:p.Met750Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360295
  ensembl transcript: ENST00000371249
  gene symbol: SORBS1
  hgvsc: ENST00000371249.2:c.2159T>C
  hgvsp: ENSP00000360295.2:p.Met720Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360271
  ensembl transcript: ENST00000371227
  gene symbol: SORBS1
  hgvsc: ENST00000371227.4:c.2675T>C
  hgvsp: ENSP00000360271.3:p.Met892Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000343998
  ensembl transcript: ENST00000353505
  gene symbol: SORBS1
  hgvsc: ENST00000353505.5:c.2366T>C
  hgvsp: ENSP00000343998.5:p.Met789Thr
  variant of: http://identifiers.org/hgnc/14565
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000095637
  ensembl protein: ENSP00000360291
  ensembl transcript: ENST00000371245
  gene symbol: SORBS1
  hgvsc: ENST00000371245.3:c.2366T>C
  hgvsp: ENSP00000360291.2:p.Met789Thr
  variant of: http://identifiers.org/hgnc/14565
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met938Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

9-134952845-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952845
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952845
    reference: chr 9
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.133A>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.332A>T
  hgvsp: ENSP00000292035.5:p.Tyr111Phe
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.332A>T
  hgvsp: ENSP00000349530.3:p.Tyr111Phe
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.332A>T
  hgvsp: ENSP00000477136.1:p.Tyr111Phe
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17404
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7063
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5057
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3740
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr111Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

9-134952845-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952845
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952845
    reference: chr 9
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.332A>G
  hgvsp: ENSP00000477136.1:p.Tyr111Cys
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.332A>G
  hgvsp: ENSP00000292035.5:p.Tyr111Cys
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.133A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.332A>G
  hgvsp: ENSP00000349530.3:p.Tyr111Cys
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3740
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17404
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17418
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr111Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

9-134952850-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952850
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952850
    reference: chr 9
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.327A>G
  hgvsp: ENST00000292035.5:c.327A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.327A>G
  hgvsp: ENST00000474263.1:c.327A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.327A>G
  hgvsp: ENST00000357028.2:c.327A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.128A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7059
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3738
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17429
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3090
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln109Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

9-134952850-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952850
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952850
    reference: chr 9
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.327A>C
  hgvsp: ENSP00000292035.5:p.Gln109His
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.128A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.327A>C
  hgvsp: ENSP00000349530.3:p.Gln109His
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.327A>C
  hgvsp: ENSP00000477136.1:p.Gln109His
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7059
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17429
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3738
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17403
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln109His
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/9-134952882-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952882
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952882
    reference: chr 9
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.295G>T
  hgvsp: ENSP00000292035.5:p.Asp99Tyr
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.295G>T
  hgvsp: ENSP00000349530.3:p.Asp99Tyr
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.295G>T
  hgvsp: ENSP00000477136.1:p.Asp99Tyr
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.96G>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3091
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5053
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17399
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7065
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17447
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp99Tyr
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

9-134952888-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952888
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952888
    reference: chr 9
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.289G>A
  hgvsp: ENSP00000349530.3:p.Val97Met
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.90G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.289G>A
  hgvsp: ENSP00000477136.1:p.Val97Met
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.289G>A
  hgvsp: ENSP00000292035.5:p.Val97Met
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17400
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3091
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4635
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17446
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5053
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val97Met
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: C
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

9-134952891-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952891
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952891
    reference: chr 9
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.286C>G
  hgvsp: ENSP00000349530.3:p.Pro96Ala
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.286C>G
  hgvsp: ENSP00000477136.1:p.Pro96Ala
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.87C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.286C>G
  hgvsp: ENSP00000292035.5:p.Pro96Ala
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3091
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17399
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3738
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7065
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17447
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro96Ala
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: G
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

9-134952907-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952907
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952907
    reference: chr 9
allele count: 123
allele frequency: 1.013196263529877e-3
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.270G>A
  hgvsp: ENST00000474263.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.270G>A
  hgvsp: ENST00000292035.5:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.71G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.270G>A
  hgvsp: ENST00000357028.2:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 9.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 13075
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13093
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6960
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 7052
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17447
  bin: 9.75e1
  variant carriers: 123
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2262
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly90Gly
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

9-134952914-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952914
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952914
    reference: chr 9
allele count: 3
allele frequency: 2.471210398853358e-5
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.263A>G
  hgvsp: ENSP00000292035.5:p.Asn88Ser
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.64A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.263A>G
  hgvsp: ENSP00000477136.1:p.Asn88Ser
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.263A>G
  hgvsp: ENSP00000349530.3:p.Asn88Ser
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17340
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3093
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3740
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7070
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4635
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asn88Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-134952916-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952916
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952916
    reference: chr 9
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.261T>G
  hgvsp: ENSP00000477136.1:p.His87Gln
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.261T>G
  hgvsp: ENSP00000292035.5:p.His87Gln
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.261T>G
  hgvsp: ENSP00000349530.3:p.His87Gln
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.62T>G
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5056
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17339
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3093
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17476
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His87Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

9-134952917-TGAAGAGGATG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952917
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952907
    reference: chr 9
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsp: ENSP00000292035.5:p.His84IlefsTer6
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsp: ENSP00000349530.3:p.His84IlefsTer6
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.51_60delCATCCTCTTC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsp: ENSP00000477136.1:p.His84IlefsTer6
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7071
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3741
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5056
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3091
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17477
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17338
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His84IlefsTer6
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: TGAAGAGGATG
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

9-134952927-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952927
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952927
    reference: chr 9
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.250C>T
  hgvsp: ENSP00000477136.1:p.His84Tyr
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.51C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.250C>T
  hgvsp: ENSP00000292035.5:p.His84Tyr
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.250C>T
  hgvsp: ENSP00000349530.3:p.His84Tyr
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6960
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3740
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17481
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3091
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5056
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His84Tyr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

9-134952939-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952939
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952939
    reference: chr 9
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.238C>G
  hgvsp: ENSP00000477136.1:p.Pro80Ala
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.238C>G
  hgvsp: ENSP00000349530.3:p.Pro80Ala
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.238C>G
  hgvsp: ENSP00000292035.5:p.Pro80Ala
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.39C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7066
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17482
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17332
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4637
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5056
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro80Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

9-134952950-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952950
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952950
    reference: chr 9
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.227T>C
  hgvsp: ENSP00000292035.5:p.Leu76Pro
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.227T>C
  hgvsp: ENSP00000477136.1:p.Leu76Pro
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.28T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.227T>C
  hgvsp: ENSP00000349530.3:p.Leu76Pro
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17330
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7061
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5057
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17456
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3739
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3086
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu76Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

9-134952951-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952951
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952951
    reference: chr 9
allele count: 7
allele frequency: 5.76710771309463e-5
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.226C>G
  hgvsp: ENSP00000349530.3:p.Leu76Val
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.226C>G
  hgvsp: ENSP00000477136.1:p.Leu76Val
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.226C>G
  hgvsp: ENSP00000292035.5:p.Leu76Val
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.27C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4636
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7063
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17330
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17459
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3739
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu76Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

9-134952960-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952960
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952960
    reference: chr 9
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.217C>T
  hgvsp: ENST00000474263.1:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.217C>T
  hgvsp: ENST00000357028.2:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.217C>T
  hgvsp: ENST00000292035.5:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.18C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3739
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7059
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4635
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3085
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17324
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5056
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu73Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

9-134952962-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952962
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952962
    reference: chr 9
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.215G>A
  hgvsp: ENSP00000349530.3:p.Arg72His
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.215G>A
  hgvsp: ENSP00000477136.1:p.Arg72His
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.16G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.215G>A
  hgvsp: ENSP00000292035.5:p.Arg72His
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17324
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7051
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3083
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4635
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg72His
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum

9-134952972-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952972
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952972
    reference: chr 9
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.6G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.205G>A
  hgvsp: ENSP00000292035.5:p.Glu69Lys
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.205G>A
  hgvsp: ENSP00000477136.1:p.Glu69Lys
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.205G>A
  hgvsp: ENSP00000349530.3:p.Glu69Lys
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5050
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3736
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7028
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17296
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu69Lys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

9-134952973-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952973
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952973
    reference: chr 9
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000230940
  ensembl transcript: ENST00000444872
  gene symbol: RP11-32B11.2
  hgvsc: ENST00000444872.2:n.5T>C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.204T>C
  hgvsp: ENST00000292035.5:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.204T>C
  hgvsp: ENST00000474263.1:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.204T>C
  hgvsp: ENST00000357028.2:c.204T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3736
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3074
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4626
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5053
  bin: 7.75e1
  variant carriers: 0
hgvs: c.204T>C
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

9-134952980-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952980
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952980
    reference: chr 9
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.204-7T>C
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.204-7T>C
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.204-7T>C
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9543
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2256
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17316
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3061
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7001
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3734
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17170
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4622
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5046
  bin: 7.75e1
  variant carriers: 0
hgvs: c.204-7T>C
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

9-134952988-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952988
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952988
    reference: chr 9
allele count: 6
allele frequency: 4.953274114189479e-5
allele num: 121132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.204-15C>A
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.204-15C>A
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.204-15C>A
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12981
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6929
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3732
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3031
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16616
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5036
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4614
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD

9-134952994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952994
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952994
    reference: chr 9
allele count: 4
allele frequency: 3.304692663582287e-5
allele num: 121040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.204-21C>T
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.204-21C>T
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.204-21C>T
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6941
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3007
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4609
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3728
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2251
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5006
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15988
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6789
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/9-134952995-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134952995
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134952995
    reference: chr 9
allele count: 4
allele frequency: 3.305675845426598e-5
allele num: 121004
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.204-22G>T
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.204-22G>T
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.204-22G>T
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4606
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2249
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6729
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2989
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15779
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17290
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3723
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

9-134953002-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134953002
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134953002
    reference: chr 9
allele count: 1
allele frequency: 8.268973158913126e-6
allele num: 120934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.204-29T>C
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.204-29T>C
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.204-29T>C
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9445
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14226
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1140
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2936
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6427
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3717
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17285
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4601
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

9-134953006-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134953006
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134953006
    reference: chr 9
allele count: 4
allele frequency: 3.309614429918914e-5
allele num: 120860
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.204-33T>C
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.204-33T>C
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.204-33T>C
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12000
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4591
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1268
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17276
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 6072
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3708
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4891
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2873
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

9-134953017-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134953017
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134953017
    reference: chr 9
allele count: 1
allele frequency: 8.299719469481931e-6
allele num: 120486
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.204-44G>A
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.204-44G>A
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.204-44G>A
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3695
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5674
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4815
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1338
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4533
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10338
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1419
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1932
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

9-134953018-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134953018
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134953018
    reference: chr 9
allele count: 72
allele frequency: 5.976194823951261e-4
allele num: 120478
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.204-45T>C
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.204-45T>C
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.204-45T>C
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9089
  bin: 3.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10424
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6859
  bin: 4.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5503
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4518
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2045
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17296
  bin: 9.75e1
  variant carriers: 72
genotype quality: GenotypeQuality
  all individuals: 3684
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4789
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2219
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum

9-134954979-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134954979
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134954979
    reference: chr 9
allele count: 1
allele frequency: 8.529075618784437e-6
allele num: 117246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.203+50C>T
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.203+50C>T
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.203+50C>T
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14474
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1921
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35095
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1586
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1790
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7600
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP

9-134954981-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134954981
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134954981
    reference: chr 9
allele count: 4
allele frequency: 3.435245620061834e-5
allele num: 116440
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.203+48A>C
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.203+48A>C
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.203+48A>C
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24260
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1960
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1661
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1652
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35452
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7322
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ

9-134954988-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 134954988
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 134954988
    reference: chr 9
allele count: 1
allele frequency: 8.665811639918195e-6
allele num: 115396
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000292035
  ensembl transcript: ENST00000292035
  gene symbol: MED27
  hgvsc: ENST00000292035.5:c.203+41C>T
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000349530
  ensembl transcript: ENST00000357028
  gene symbol: MED27
  hgvsc: ENST00000357028.2:c.203+41C>T
  variant of: http://identifiers.org/hgnc/2377
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160563
  ensembl protein: ENSP00000477136
  ensembl transcript: ENST00000474263
  gene symbol: MED27
  hgvsc: ENST00000474263.1:c.203+41C>T
  variant of: http://identifiers.org/hgnc/2377
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 4781
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2547
bin: 3.25e1
variant carriers: 1

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

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

GenotypeDepth
all individuals: 8
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5558
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 239
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 340
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8416
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 662
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4094
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39504
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 9.75e1
variant carriers: 8

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10498
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.532888465204957e-4
allele num: 8392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11072
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8856
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.123e0

QD
type: SiteQuality
SIO_000300: 1.17e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.23e-1

DP
type: SiteQuality
SIO_000300: 1.264342e6

GenotypeDepth
all individuals: 1639
bin: 1.75e1
variant carriers: 0

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

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

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

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

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

GenotypeDepth
all individuals: 3
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8607
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4115
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40074
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11072
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.627869119322807e-5
allele num: 61430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5872
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

MQ
type: SiteQuality
SIO_000300: 5.896e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.878e0

QD
type: SiteQuality
SIO_000300: 1.913e1

FS
type: SiteQuality
SIO_000300: 2.375e0

DP
type: SiteQuality
SIO_000300: 1.260173e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

GenotypeDepth
all individuals: 1518
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5710
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 359
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8700
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39845
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4115
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1706
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5848
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.193887297039159e-4
allele num: 8376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8766
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.323e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.165e0

DP
type: SiteQuality
SIO_000300: 1.255976e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.16e-1

QD
type: SiteQuality
SIO_000300: 5.81e0

FS
type: SiteQuality
SIO_000300: 1.3054e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.15e-1

GenotypeDepth
all individuals: 221
bin: 3.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 4927
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14190
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1706
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 199
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 611
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4115
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39845
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8700
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.632120124041129e-5
allele num: 61270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.255976e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.323e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.165e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.55e-1

FS
type: SiteQuality
SIO_000300: 1.3054e1

QD
type: SiteQuality
SIO_000300: 5.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.16e-1

GenotypeDepth
all individuals: 13342
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2217
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6716
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 210
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 21
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 455
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36128
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9606
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5676
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10760
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.682708487581611e-5
allele num: 59428
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.205e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.05e-1

DP
type: SiteQuality
SIO_000300: 1.212903e6

QD
type: SiteQuality
SIO_000300: 1.101e1

FS
type: SiteQuality
SIO_000300: 2.791e0

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

GenotypeDepth
all individuals: 5681
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 13342
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9606
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36128
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.21153380179307e-4
allele num: 8254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5676
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59428
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.212903e6

QD
type: SiteQuality
SIO_000300: 1.101e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-1

FS
type: SiteQuality
SIO_000300: 2.791e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.205e0

GenotypeDepth
all individuals: 45
bin: 4.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13079
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 27508
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 153
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35734
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9753
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 490
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 817
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2538
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3477
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.220107369448512e-4
allele num: 8196
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.187165049860932e-4
allele num: 58964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9330
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 1.456e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

QD
type: SiteQuality
SIO_000300: 8.56e0

DP
type: SiteQuality
SIO_000300: 1.203101e6

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

GenotypeDepth
all individuals: 27425
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 20
bin: 4.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 1187
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2625
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3446
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 744
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9831
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34905
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5588
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.384384384384384e-5
allele num: 10656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.113868812218738e-5
allele num: 58664
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9166
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

QD
type: SiteQuality
SIO_000300: 1.405e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

FS
type: SiteQuality
SIO_000300: 6.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.99e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

MQRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.194479e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e-1

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

GenotypeDepth
all individuals: 27575
bin: 2.25e1
variant carriers: 3

GenotypeDepth
all individuals: 189
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 12710
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3369
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10175
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35786
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.707883590654461e-5
allele num: 58552
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 1.096250822188117e-3
allele num: 9122
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.193085e6

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

MQ
type: SiteQuality
SIO_000300: 5.907e1

VQSLOD
type: SiteQuality
SIO_000300: -4.258e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

FS
type: SiteQuality
SIO_000300: 7.623e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

GenotypeDepth
all individuals: 12377
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 27596
bin: 2.25e1
variant carriers: 3

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

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

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

GenotypeDepth
all individuals: 23
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 230
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10524
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3376
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 632
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2718
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35436
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10602
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.684598378776713e-4
allele num: 8142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.713796058269066e-5
allele num: 58350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9052
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

FS
type: SiteQuality
SIO_000300: 1.182e0

DP
type: SiteQuality
SIO_000300: 1.184426e6

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.53e-1

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

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

GenotypeDepth
all individuals: 27805
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6077
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2802
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 4.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 2203
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3199
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11546
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2921
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35396
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 664
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8076
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57664
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10462
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

MQ
type: SiteQuality
SIO_000300: 5.951e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.77e-1

DP
type: SiteQuality
SIO_000300: 1.161267e6

GenotypeDepth
all individuals: 17
bin: 4.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 1
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27520
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11451
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3007
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3153
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11933
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1127
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35165
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.741250217656277e-5
allele num: 57430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5358
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.288e1

MQRankSum
type: SiteQuality
SIO_000300: -2.164e0

FS
type: SiteQuality
SIO_000300: 1.062e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.867e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.155004e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

GenotypeDepth
all individuals: 31
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1879
bin: 3.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 18
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 427
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1539
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3644
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 543
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16047
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29309
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7978
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5042
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.319609395618897e-4
allele num: 7578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7700
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.084026e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.03e-1

QD
type: SiteQuality
SIO_000300: 1.572e1

FS
type: SiteQuality
SIO_000300: 6.276e0

VQSLOD
type: SiteQuality
SIO_000300: 2.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.389999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeDepth
all individuals: 3513
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 4.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 22849
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 117
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 831
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1367
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16179
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3638
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29783
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7968
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.830027084400849e-5
allele num: 54644
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 656
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5034
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.738e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

QD
type: SiteQuality
SIO_000300: 7.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

FS
type: SiteQuality
SIO_000300: 1.612e0

DP
type: SiteQuality
SIO_000300: 1.082824e6

MQ
type: SiteQuality
SIO_000300: 5.919e1

GenotypeDepth
all individuals: 11355
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 4.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1528
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 9486
bin: 2.75e1
variant carriers: 4

GenotypeDepth
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 793
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19512
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 9.75e1
variant carriers: 26

GenotypeQuality
all individuals: 557
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1711
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4298
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1452
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26476
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.07641196013289e-4
allele num: 4816
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 4.806028682379177e-4
allele num: 52018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7250
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7446
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.362e0

FS
type: SiteQuality
SIO_000300: 7.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.1e0

DP
type: SiteQuality
SIO_000300: 1.021703e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

QD
type: SiteQuality
SIO_000300: 1.28e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

GenotypeDepth
all individuals: 8563
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 471
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9047
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3252
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35071
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 912
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5314
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2062
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4932
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5988
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4702
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.14e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

QD
type: SiteQuality
SIO_000300: 7.5e0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 4.771e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.638e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-1

DP
type: SiteQuality
SIO_000300: 6.43331e5

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

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

GenotypeDepth
all individuals: 18
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 7.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1433
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14356
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30124
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2835
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2881
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 193
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2136
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 8.210180623973727e-4
allele num: 3654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3062
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.073e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

QD
type: SiteQuality
SIO_000300: 1.468e1

VQSLOD
type: SiteQuality
SIO_000300: -1.268e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.94e-1

DP
type: SiteQuality
SIO_000300: 5.10444e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.12e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

GenotypeDepth
all individuals: 20825
bin: 2.5e0
variant carriers: 0

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

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

GenotypeDepth
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1742
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15544
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5421
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1935
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7020
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20943
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3027
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1916
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1282
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.19672131147541e-4
allele num: 1220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1322
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.191e0

MQRankSum
type: SiteQuality
SIO_000300: -1.191e0

DP
type: SiteQuality
SIO_000300: 3.66663e5

VQSLOD
type: SiteQuality
SIO_000300: -1.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.73e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.91e0

GenotypeDepth
all individuals: 20840
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7783
bin: 1.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1261
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 194
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7416
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6259
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20674
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14095
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 179
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1701
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 5.44069640914037e-4
allele num: 1838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1158
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.829e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.354e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

DP
type: SiteQuality
SIO_000300: 3.63668e5

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.88e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.82e0

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

GenotypeDepth
all individuals: 27208
bin: 7.5e0
variant carriers: 2

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

GenotypeDepth
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18898
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1803
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 665
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10134
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8008
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5495
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9345
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1663
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 998
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1120
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 950
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.519e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.263e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 3.58693e5

GenotypeDepth
all individuals: 1300
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2606
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9259
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 637
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 5627
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1623
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1355
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5529
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8297
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23423
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2714
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3834
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4499
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.661425153050126e-5
allele num: 64358
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: -1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

QD
type: SiteQuality
SIO_000300: 1.151e1

FS
type: SiteQuality
SIO_000300: 1.4004e1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.663e0

DP
type: SiteQuality
SIO_000300: 2.513149e6

GenotypeDepth
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1300
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7912
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3962
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 794
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1803
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10395
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1624
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4731
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 622
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2715
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2032
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4498
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5532
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8316
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23420
bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64370
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.828864537188156e-4
allele num: 8578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.216e0

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

DP
type: SiteQuality
SIO_000300: 2.514966e6

QD
type: SiteQuality
SIO_000300: 1.553e1

GenotypeDepth
all individuals: 1317
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 415
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6739
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5627
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1619
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1301
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 255
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2737
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4498
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2715
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23421
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8333
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5532
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4729
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 1.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 6.9e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.517522e6

VQSLOD
type: SiteQuality
SIO_000300: -1.53e0

GenotypeDepth
all individuals: 635
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6743
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1302
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 793
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2604
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 415
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4496
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8414
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3235
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23423
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64552
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.742790335151988e-5
allele num: 10264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 2.524165e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.066e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.1e-2

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.068e1

GenotypeDepth
all individuals: 111
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9261
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3963
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7913
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1803
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 415
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1302
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 886
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23423
bin: 9.75e1
variant carriers: 10

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

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 151
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4496
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3235
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8414
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.948558067030398e-4
allele num: 10264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549138678894535e-5
allele num: 64552
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.147113594040968e-4
allele num: 8592
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

FS
type: SiteQuality
SIO_000300: 5.77e-1

DP
type: SiteQuality
SIO_000300: 2.524165e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.066e0

QD
type: SiteQuality
SIO_000300: 1.068e1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeDepth
all individuals: 6744
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 415
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 932
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1621
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 9262
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2605
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1803
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3331
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8452
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4496
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5539
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23418
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2283
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.738261057975052e-5
allele num: 64614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10478
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

DP
type: SiteQuality
SIO_000300: 2.524924e6

FS
type: SiteQuality
SIO_000300: 2.726e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.29e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.94e-1

GenotypeDepth
all individuals: 937
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5629
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 415
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3964
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1081
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 792
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1617
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 356
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4496
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8574
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2717
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5544
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23416
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3422
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64700
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10736
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.322880371660859e-4
allele num: 8610
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.01e-1

DP
type: SiteQuality
SIO_000300: 2.528319e6

MQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.304e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

FS
type: SiteQuality
SIO_000300: 1.242e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.973e0

GenotypeDepth
all individuals: 6778
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1431
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3964
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 414
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 792
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3233
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7914
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 963
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10397
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1804
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2606
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 531
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1300
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8920
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23416
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4497
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3288
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2724
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4735
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5556
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.735150244584206e-5
allele num: 11448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64970
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.069e1

VQSLOD
type: SiteQuality
SIO_000300: 2.56e-1

FS
type: SiteQuality
SIO_000300: 3.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.138e0

DP
type: SiteQuality
SIO_000300: 2.535646e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.359e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

GenotypeDepth
all individuals: 634
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 414
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3031
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 994
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1300
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2606
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 963
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10397
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1616
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1581
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5560
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3078
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4734
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4497
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23415
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 349
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8995
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.677542519958348e-5
allele num: 11524
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.688044952528579e-5
allele num: 10322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65096
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11658
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.74e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.187e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

QD
type: SiteQuality
SIO_000300: 1.36e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.679e0

DP
type: SiteQuality
SIO_000300: 2.53918e6

MQ
type: SiteQuality
SIO_000300: 5.986e1

GenotypeDepth
all individuals: 3964
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 886
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6940
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5630
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1614
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2606
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1804
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 414
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1300
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 963
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 791
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4500
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23416
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9775
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4741
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5590
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.047108294228777e-5
allele num: 65636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
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: 850
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.554144e6

MQ
type: SiteQuality
SIO_000300: 5.939e1

QD
type: SiteQuality
SIO_000300: 1.165e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

FS
type: SiteQuality
SIO_000300: 1.736e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e-1

GenotypeDepth
all individuals: 791
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 818
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5631
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1804
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 414
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2584
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1613
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 963
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 369
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 10418
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10100
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3834
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 225
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23416
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2170
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4500
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5619
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4745
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.535795026375282e-5
allele num: 13270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65778
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

QD
type: SiteQuality
SIO_000300: 8.15e0

VQSLOD
type: SiteQuality
SIO_000300: -6.44e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.557469e6

GenotypeDepth
all individuals: 5631
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1300
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2606
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2779
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 532
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 343
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1804
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3964
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 963
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9265
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10309
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5626
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4746
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23417
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3833
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2729
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4500
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 2.228163992869875e-4
allele num: 13464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65838
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.560824e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

QD
type: SiteQuality
SIO_000300: 1.09e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

FS
type: SiteQuality
SIO_000300: 3.322e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.017e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
all individuals: 9263
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 962
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1692
bin: 7.5e0
variant carriers: 3

GenotypeDepth
all individuals: 7057
bin: 2.75e1
variant carriers: 11

GenotypeDepth
all individuals: 693
bin: 1.25e1
variant carriers: 8

GenotypeDepth
all individuals: 3959
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 413
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 635
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 1801
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 531
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 226
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4498
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2284
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4747
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5655
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2732
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10581
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 202
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23457
bin: 9.75e1
variant carriers: 87

South Asian
type: Population
allele count: 85
allele frequency: 6.141618497109827e-3
allele num: 13840
num of homozygotes: 1

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.162790697674419e-3
allele num: 860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516162290011523e-5
allele num: 65956
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.47e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.91e-1

DP
type: SiteQuality
SIO_000300: 2.56717e6

FS
type: SiteQuality
SIO_000300: 5.2e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

QD
type: SiteQuality
SIO_000300: 1.259e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.528e0

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

GenotypeDepth
all individuals: 7074
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 307
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 633
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10442
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 664
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3131
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 786
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5633
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9272
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3960
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2735
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4757
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10638
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23380
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5670
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2285
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3835
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4502
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
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: 13938
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515748628247491e-5
allele num: 65974
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 2.565018e6

MQRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.273e1

FS
type: SiteQuality
SIO_000300: 5.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeDepth
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5633
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10442
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3960
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 962
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 786
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1609
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7907
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1801
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 633
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2604
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5670
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4757
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2285
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23380
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3835
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2735
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10638
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4502
bin: 8.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
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: 3
allele frequency: 2.152389151958674e-4
allele num: 13938
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65974
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.273e1

MQRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

FS
type: SiteQuality
SIO_000300: 5.05e0

DP
type: SiteQuality
SIO_000300: 2.565018e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

GenotypeDepth
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 305
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7085
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 638
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10443
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1297
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3960
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7907
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1608
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3835
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4503
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23378
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 206
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1671
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5668
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2733
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14020
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: 862
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.346e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.349e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

DP
type: SiteQuality
SIO_000300: 2.566049e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.49e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

GenotypeDepth
all individuals: 632
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7907
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3960
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 617
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7095
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1801
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1297
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1607
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 786
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10865
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3835
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2285
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2742
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4504
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5668
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4754
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23377
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14108
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514096235956757e-5
allele num: 66046
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.923e1

DP
type: SiteQuality
SIO_000300: 2.567072e6

VQSLOD
type: SiteQuality
SIO_000300: -7.74e-2

FS
type: SiteQuality
SIO_000300: 1.0109e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

QD
type: SiteQuality
SIO_000300: 1.295e1

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

GenotypeDepth
all individuals: 1801
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7908
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7549
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4319
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2605
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9275
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1606
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 643
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4766
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3835
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 23378
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 97
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4507
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5771
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12230
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504438092372499e-5
allele num: 66470
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.66e-1

DP
type: SiteQuality
SIO_000300: 2.588882e6

FS
type: SiteQuality
SIO_000300: 3.522e0

QD
type: SiteQuality
SIO_000300: 1.444e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-3

GenotypeDepth
all individuals: 10511
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 631
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1801
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 785
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7644
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4401
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 413
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 9276
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3836
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12543
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23376
bin: 9.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4768
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5785
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4505
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 2.25e1
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15794
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66514
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.779010633379565e-4
allele num: 8652
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

DP
type: SiteQuality
SIO_000300: 2.592281e6

MQRankSum
type: SiteQuality
SIO_000300: -5.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17418
bin: 6.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
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: 66728
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.789e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.44e-1

MQ
type: SiteQuality
SIO_000300: 5.239e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.82e0

DP
type: SiteQuality
SIO_000300: 2.35113e6

VQSLOD
type: SiteQuality
SIO_000300: -1.028e0

QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeQuality
all individuals: 7063
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5057
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.028e0

DP
type: SiteQuality
SIO_000300: 2.35113e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.44e-1

FS
type: SiteQuality
SIO_000300: 2.789e0

MQ
type: SiteQuality
SIO_000300: 5.239e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.44e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17403
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5055
bin: 7.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.466605038132656e-4
allele num: 8654
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.1e-1

DP
type: SiteQuality
SIO_000300: 2.3513e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.44e-1

MQ
type: SiteQuality
SIO_000300: 5.123e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

QD
type: SiteQuality
SIO_000300: 1.289e1

VQSLOD
type: SiteQuality
SIO_000300: -1.029e0

MQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

GenotypeQuality
all individuals: 5055
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3090
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.1e-1

DP
type: SiteQuality
SIO_000300: 2.3513e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.123e1

MQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

QD
type: SiteQuality
SIO_000300: 1.289e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.029e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

GenotypeQuality
all individuals: 4636
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3738
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

VQSLOD
type: SiteQuality
SIO_000300: -1.155e0

MQ
type: SiteQuality
SIO_000300: 4.382e1

FS
type: SiteQuality
SIO_000300: 2.261e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.566e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.56e-1

DP
type: SiteQuality
SIO_000300: 2.351072e6

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

GenotypeQuality
all individuals: 3738
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7065
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 906
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.350817e6

QD
type: SiteQuality
SIO_000300: 1.546e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.104e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.893e0

MQ
type: SiteQuality
SIO_000300: 3.924e1

FS
type: SiteQuality
SIO_000300: 1.5688e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.251e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-2

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

GenotypeQuality
all individuals: 4635
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5054
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 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: 10406
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

MQ
type: SiteQuality
SIO_000300: 3.584e1

VQSLOD
type: SiteQuality
SIO_000300: -2.741e0

DP
type: SiteQuality
SIO_000300: 2.350784e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

GenotypeQuality
all individuals: 3736
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5047
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 104
allele frequency: 6.298449612403101e-3
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.454828122300915e-4
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.098069775806258e-4
allele num: 66728
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: -3.873e0

DP
type: SiteQuality
SIO_000300: 2.352759e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.303e0

FS
type: SiteQuality
SIO_000300: 1.234e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-1

MQ
type: SiteQuality
SIO_000300: 3.585e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.03e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

GenotypeQuality
all individuals: 5057
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17482
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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

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

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-2

DP
type: SiteQuality
SIO_000300: 2.345948e6

MQ
type: SiteQuality
SIO_000300: 3.946e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

QD
type: SiteQuality
SIO_000300: 1.296e1

VQSLOD
type: SiteQuality
SIO_000300: -2.384e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.73e-1

GenotypeQuality
all individuals: 2265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3741
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7072
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -3.756e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 3.473e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e0

DP
type: SiteQuality
SIO_000300: 2.34573e6

QD
type: SiteQuality
SIO_000300: 1.155e1

FS
type: SiteQuality
SIO_000300: 5.524e0

MQRankSum
type: SiteQuality
SIO_000300: -1.645e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 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: 10406
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: 8652
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 3.76e1

DP
type: SiteQuality
SIO_000300: 2.345736e6

QD
type: SiteQuality
SIO_000300: 2.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.223e0

MQRankSum
type: SiteQuality
SIO_000300: -4.205e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.85e-1

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17337
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7070
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.353e1

FS
type: SiteQuality
SIO_000300: 4.393e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.029e0

MQ
type: SiteQuality
SIO_000300: 4.108e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

DP
type: SiteQuality
SIO_000300: 2.34569e6

MQRankSum
type: SiteQuality
SIO_000300: 2.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.938e0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3739
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.62e-2

MQ
type: SiteQuality
SIO_000300: 4.374e1

MQRankSum
type: SiteQuality
SIO_000300: -5.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.325e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.345375e6

QD
type: SiteQuality
SIO_000300: 2.291e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
all individuals: 4635
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 4.882e1

FS
type: SiteQuality
SIO_000300: 6.39e0

VQSLOD
type: SiteQuality
SIO_000300: -9.607e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.58e-1

DP
type: SiteQuality
SIO_000300: 2.344976e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-1

QD
type: SiteQuality
SIO_000300: 1.184e1

MQRankSum
type: SiteQuality
SIO_000300: -1.486e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5057
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 7
allele frequency: 6.045949214026602e-4
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e-1

DP
type: SiteQuality
SIO_000300: 2.344838e6

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

FS
type: SiteQuality
SIO_000300: 6.05e-1

MQ
type: SiteQuality
SIO_000300: 4.846e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.342e0

QD
type: SiteQuality
SIO_000300: 1.355e1

GenotypeQuality
all individuals: 2264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17432
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 3.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.039e0

MQ
type: SiteQuality
SIO_000300: 5.082e1

DP
type: SiteQuality
SIO_000300: 2.343965e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

VQSLOD
type: SiteQuality
SIO_000300: -1.956e0

GenotypeQuality
all individuals: 17404
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5054
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3738
bin: 9.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.343956e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

FS
type: SiteQuality
SIO_000300: 2.536e0

MQ
type: SiteQuality
SIO_000300: 5.461e1

QD
type: SiteQuality
SIO_000300: 1.353e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.06e0

MQRankSum
type: SiteQuality
SIO_000300: 7.85e-1

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

GenotypeQuality
all individuals: 4626
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17321
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2259
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.51e0

QD
type: SiteQuality
SIO_000300: 6.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.37e-1

FS
type: SiteQuality
SIO_000300: 7.469e0

MQ
type: SiteQuality
SIO_000300: 5.376e1

VQSLOD
type: SiteQuality
SIO_000300: -1.541e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.36e-1

DP
type: SiteQuality
SIO_000300: 2.342059e6

GenotypeQuality
all individuals: 7038
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17320
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17306
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
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

VQSLOD
type: SiteQuality
SIO_000300: -1.951e0

MQRankSum
type: SiteQuality
SIO_000300: -6.05e-1

DP
type: SiteQuality
SIO_000300: 2.341938e6

FS
type: SiteQuality
SIO_000300: 1.3476e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e-1

MQ
type: SiteQuality
SIO_000300: 5.469e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

QD
type: SiteQuality
SIO_000300: 1.168e1

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 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
allele num: 6614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.518e0

QD
type: SiteQuality
SIO_000300: 1.604e1

MQ
type: SiteQuality
SIO_000300: 4.704e1

VQSLOD
type: SiteQuality
SIO_000300: -1.74e0

DP
type: SiteQuality
SIO_000300: 2.339275e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.59e-1

GenotypeQuality
all individuals: 17309
bin: 9.75e1
variant carriers: 6

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
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

East Asian
type: Population
allele count: 5
allele frequency: 5.792400370713623e-4
allele num: 8632
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.204e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.02e-1

DP
type: SiteQuality
SIO_000300: 2.331789e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.086e0

MQ
type: SiteQuality
SIO_000300: 5.379e1

FS
type: SiteQuality
SIO_000300: 7.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.09e-1

QD
type: SiteQuality
SIO_000300: 1.087e1

GenotypeQuality
all individuals: 17297
bin: 9.75e1
variant carriers: 4

South Asian
type: Population
allele count: 4
allele frequency: 2.450079627587897e-4
allele num: 16326
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: 10402
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.639e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQ
type: SiteQuality
SIO_000300: 5.587e1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 1.8492e1

DP
type: SiteQuality
SIO_000300: 2.321959e6

VQSLOD
type: SiteQuality
SIO_000300: -2.926e0

QD
type: SiteQuality
SIO_000300: 1.601e1

GenotypeQuality
all individuals: 4984
bin: 7.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.455494168201351e-4
allele num: 16290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

DP
type: SiteQuality
SIO_000300: 2.319707e6

VQSLOD
type: SiteQuality
SIO_000300: -2.039e0

MQ
type: SiteQuality
SIO_000300: 5.258e1

FS
type: SiteQuality
SIO_000300: 1.1984e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.233e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.909e0

GenotypeQuality
all individuals: 4951
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501907422426482e-5
allele num: 66582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.495e1

DP
type: SiteQuality
SIO_000300: 2.297945e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.315e0

MQRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQ
type: SiteQuality
SIO_000300: 5.227e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.416e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.78e0

GenotypeQuality
all individuals: 347
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66560
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 902
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.647920055775041e-4
allele num: 8606
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

MQRankSum
type: SiteQuality
SIO_000300: -2.75e-1

QD
type: SiteQuality
SIO_000300: 1.44e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.28245e6

MQ
type: SiteQuality
SIO_000300: 5.257e1

VQSLOD
type: SiteQuality
SIO_000300: -1.087e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
all individuals: 17256
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16024
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505389293671343e-5
allele num: 66428
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.381e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQRankSum
type: SiteQuality
SIO_000300: -4.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.702e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.766e0

QD
type: SiteQuality
SIO_000300: 8.550000000000001e0

FS
type: SiteQuality
SIO_000300: 3.757e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-1

DP
type: SiteQuality
SIO_000300: 2.245472e6

GenotypeQuality
all individuals: 9181
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 1.211491865697473e-3
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 55
allele frequency: 8.281635848942962e-4
allele num: 66412
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.2271714922049e-3
allele num: 898
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16058
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.52e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.55e-1

DP
type: SiteQuality
SIO_000300: 2.239567e6

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

MQ
type: SiteQuality
SIO_000300: 5.38e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.465e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.74e0

GenotypeQuality
all individuals: 1438
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558166349839509e-5
allele num: 64178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.063e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.48e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 9.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.445e0

DP
type: SiteQuality
SIO_000300: 1.611508e6

GenotypeQuality
all individuals: 284
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.088850174216028e-4
allele num: 9184
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.730574471800244e-5
allele num: 11454
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.137058066944819e-5
allele num: 63754
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8324
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.117e0

FS
type: SiteQuality
SIO_000300: 2.3618e1

DP
type: SiteQuality
SIO_000300: 1.603432e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.848e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-2

QD
type: SiteQuality
SIO_000300: 3.9e-1

MQ
type: SiteQuality
SIO_000300: 5.722e1