13-95686854-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95686854
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 95686854
    reference: chr 13
allele count: 1
allele frequency: 8.350172848577966e-6
allele num: 119758
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000366084
  ensembl transcript: ENST00000376887
  gene symbol: ABCC4
  hgvsc: ENST00000376887.4:c.3870+5G>A
  variant of: http://identifiers.org/hgnc/55
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000388657
  ensembl transcript: ENST00000412704
  gene symbol: ABCC4
  hgvsc: ENST00000412704.1:c.3729+5G>A
  variant of: http://identifiers.org/hgnc/55
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4240
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8025
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1306
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32481
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3027
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4659
  bin: 9.75e1
  variant carriers: 1
hgvs: c.3870+5G>A
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10302
  num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

11-129785667-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785667
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785667
    reference: chr 11
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1565C>T
  hgvsp: ENSP00000435940.1:p.Pro522Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2336C>T
  hgvsp: ENSP00000431262.1:p.Pro779Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2168C>T
  hgvsp: ENSP00000432237.1:p.Pro723Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2168C>T
  hgvsp: ENSP00000398431.2:p.Pro723Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2414C>T
  hgvsp: ENSP00000354118.3:p.Pro805Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2426C>T
  hgvsp: ENSP00000351686.5:p.Pro809Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2156C>T
  hgvsp: ENSP00000302669.6:p.Pro719Leu
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2733
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9334
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1953
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 8.75e1
  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: 2691
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro809Leu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

11-129785671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785671
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785671
    reference: chr 11
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2332C>T
  hgvsp: ENSP00000431262.1:p.Arg778Ter
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2422C>T
  hgvsp: ENSP00000351686.5:p.Arg808Ter
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2410C>T
  hgvsp: ENSP00000354118.3:p.Arg804Ter
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1561C>T
  hgvsp: ENSP00000435940.1:p.Arg521Ter
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2164C>T
  hgvsp: ENSP00000432237.1:p.Arg722Ter
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2152C>T
  hgvsp: ENSP00000302669.6:p.Arg718Ter
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2164C>T
  hgvsp: ENSP00000398431.2:p.Arg722Ter
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1953
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3737
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1244
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg808Ter
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

11-129785680-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785680
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785680
    reference: chr 11
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2323C>T
  hgvsp: ENSP00000431262.1:p.Arg775Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2155C>T
  hgvsp: ENSP00000432237.1:p.Arg719Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2413C>T
  hgvsp: ENSP00000351686.5:p.Arg805Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2401C>T
  hgvsp: ENSP00000354118.3:p.Arg801Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1552C>T
  hgvsp: ENSP00000435940.1:p.Arg518Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2143C>T
  hgvsp: ENSP00000302669.6:p.Arg715Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2155C>T
  hgvsp: ENSP00000398431.2:p.Arg719Trp
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8339
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31881
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg805Trp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

11-129785687-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785687
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785687
    reference: chr 11
allele count: 4
allele frequency: 3.295707341188102e-5
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1545G>A
  hgvsp: ENST00000533431.1:c.1545G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2148G>A
  hgvsp: ENST00000526082.1:c.2148G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2148G>A
  hgvsp: ENST00000423662.2:c.2148G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2136G>A
  hgvsp: ENST00000304538.6:c.2136G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2406G>A
  hgvsp: ENST00000358825.5:c.2406G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2394G>A
  hgvsp: ENST00000360871.3:c.2394G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2316G>A
  hgvsp: ENST00000528746.1:c.2316G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3739
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9334
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  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
hgvs: p.Pro802Pro
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: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

11-129785688-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785688
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785688
    reference: chr 11
allele count: 3
allele frequency: 2.471739775236463e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2315C>T
  hgvsp: ENSP00000431262.1:p.Pro772Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2147C>T
  hgvsp: ENSP00000398431.2:p.Pro716Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2393C>T
  hgvsp: ENSP00000354118.3:p.Pro798Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2405C>T
  hgvsp: ENSP00000351686.5:p.Pro802Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2147C>T
  hgvsp: ENSP00000432237.1:p.Pro716Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1544C>T
  hgvsp: ENSP00000435940.1:p.Pro515Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2135C>T
  hgvsp: ENSP00000302669.6:p.Pro712Leu
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3738
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  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: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31881
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2731
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro802Leu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

13-95686860-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95686860
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 95686860
    reference: chr 13
allele count: 1
allele frequency: 8.313519445321983e-6
allele num: 120286
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000366084
  ensembl transcript: ENST00000376887
  gene symbol: ABCC4
  hgvsc: ENST00000376887.4:c.3869A>G
  hgvsp: ENSP00000366084.4:p.Gln1290Arg
  variant of: http://identifiers.org/hgnc/55
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000388657
  ensembl transcript: ENST00000412704
  gene symbol: ABCC4
  hgvsc: ENST00000412704.1:c.3728A>G
  hgvsp: ENSP00000388657.1:p.Gln1243Arg
  variant of: http://identifiers.org/hgnc/55
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8168
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3305
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4699
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4368
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32644
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3127
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln1290Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

13-95686864-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95686864
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 95686864
    reference: chr 13
allele count: 1
allele frequency: 8.294212298657997e-6
allele num: 120566
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000366084
  ensembl transcript: ENST00000376887
  gene symbol: ABCC4
  hgvsc: ENST00000376887.4:c.3865A>G
  hgvsp: ENSP00000366084.4:p.Lys1289Glu
  variant of: http://identifiers.org/hgnc/55
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000388657
  ensembl transcript: ENST00000412704
  gene symbol: ABCC4
  hgvsc: ENST00000412704.1:c.3724A>G
  hgvsp: ENSP00000388657.1:p.Lys1242Glu
  variant of: http://identifiers.org/hgnc/55
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32903
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3334
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4712
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4402
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8214
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys1289Glu
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10336
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

13-95686866-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95686866
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 95686866
    reference: chr 13
allele count: 1
allele frequency: 8.28953694646617e-6
allele num: 120634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000388657
  ensembl transcript: ENST00000412704
  gene symbol: ABCC4
  hgvsc: ENST00000412704.1:c.3722C>T
  hgvsp: ENSP00000388657.1:p.Ala1241Val
  variant of: http://identifiers.org/hgnc/55
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000366084
  ensembl transcript: ENST00000376887
  gene symbol: ABCC4
  hgvsc: ENST00000376887.4:c.3863C>T
  hgvsp: ENSP00000366084.4:p.Ala1288Val
  variant of: http://identifiers.org/hgnc/55
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32890
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3338
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4715
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8213
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1645
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala1288Val
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6570
  num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

13-95686877-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95686877
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 95686877
    reference: chr 13
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000366084
  ensembl transcript: ENST00000376887
  gene symbol: ABCC4
  hgvsc: ENST00000376887.4:c.3852C>T
  hgvsp: ENST00000376887.4:c.3852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/55
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000388657
  ensembl transcript: ENST00000412704
  gene symbol: ABCC4
  hgvsc: ENST00000412704.1:c.3711C>T
  hgvsp: ENST00000412704.1:c.3711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/55
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4501
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3262
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 8300
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genotype quality: GenotypeQuality
  all individuals: 50
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genotype quality: GenotypeQuality
  all individuals: 3387
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu1284Leu
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 906
  num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

13-95686880-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95686880
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 95686880
    reference: chr 13
allele count: 3
allele frequency: 2.479420807299415e-5
allele num: 120996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000388657
  ensembl transcript: ENST00000412704
  gene symbol: ABCC4
  hgvsc: ENST00000412704.1:c.3708C>T
  hgvsp: ENST00000412704.1:c.3708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/55
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000125257
  ensembl protein: ENSP00000366084
  ensembl transcript: ENST00000376887
  gene symbol: ABCC4
  hgvsc: ENST00000376887.4:c.3849C>T
  hgvsp: ENST00000376887.4:c.3849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/55
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 185
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4518
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala1283Ala
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6584
  num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-129785693-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785693
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785693
    reference: chr 11
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2400C>A
  hgvsp: ENST00000358825.5:c.2400C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2142C>A
  hgvsp: ENST00000423662.2:c.2142C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2310C>A
  hgvsp: ENST00000528746.1:c.2310C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2130C>A
  hgvsp: ENST00000304538.6:c.2130C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2142C>A
  hgvsp: ENST00000526082.1:c.2142C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2388C>A
  hgvsp: ENST00000360871.3:c.2388C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1539C>A
  hgvsp: ENST00000533431.1:c.1539C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3737
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7067
  bin: 9.75e1
  variant carriers: 1
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: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9333
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu800Leu
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

11-129785708-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785708
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785708
    reference: chr 11
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2127C>T
  hgvsp: ENST00000423662.2:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2385C>T
  hgvsp: ENST00000358825.5:c.2385C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2115C>T
  hgvsp: ENST00000304538.6:c.2115C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2295C>T
  hgvsp: ENST00000528746.1:c.2295C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2127C>T
  hgvsp: ENST00000526082.1:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2373C>T
  hgvsp: ENST00000360871.3:c.2373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1524C>T
  hgvsp: ENST00000533431.1:c.1524C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14038
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7066
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3734
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His795His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-129785726-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785726
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785726
    reference: chr 11
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2109C>G
  hgvsp: ENST00000526082.1:c.2109C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2355C>G
  hgvsp: ENST00000360871.3:c.2355C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2277C>G
  hgvsp: ENST00000528746.1:c.2277C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2109C>G
  hgvsp: ENST00000423662.2:c.2109C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1506C>G
  hgvsp: ENST00000533431.1:c.1506C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2367C>G
  hgvsp: ENST00000358825.5:c.2367C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2097C>G
  hgvsp: ENST00000304538.6:c.2097C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1244
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9316
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7064
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31798
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala789Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

11-129785759-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785759
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785759
    reference: chr 11
allele count: 1
allele frequency: 8.318221896887321e-6
allele num: 120218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2080-4G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2068-4G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2248-4G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2080-4G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2326-4G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2338-4G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1477-4G>A
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4653
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2697
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8886
  bin: 6.75e1
  variant carriers: 0
hgvs: c.2338-4G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

11-129785764-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785764
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785764
    reference: chr 11
allele count: 1
allele frequency: 8.325701440346349e-6
allele num: 120110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2080-9C>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1477-9C>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2248-9C>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2080-9C>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2068-9C>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2326-9C>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2338-9C>A
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3622
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-129785769-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785769
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785769
    reference: chr 11
allele count: 1
allele frequency: 8.348639171814994e-6
allele num: 119780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2080-14G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2326-14G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1477-14G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2080-14G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2338-14G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2248-14G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2068-14G>A
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2686
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2536
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3607
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1940
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28805
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: FS

11-129785770-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785770
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785770
    reference: chr 11
allele count: 2
allele frequency: 1.670453026860885e-5
allele num: 119728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2080-15C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2080-15C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2326-15C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1477-15C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2068-15C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2248-15C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2338-15C>T
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2978
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

11-129785773-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785773
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785773
    reference: chr 11
allele count: 1
allele frequency: 8.359246999030327e-6
allele num: 119628
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1477-18A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2080-18A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2326-18A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2338-18A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2068-18A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2080-18A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2248-18A>G
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7027
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2679
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-129785791-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785791
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785791
    reference: chr 11
allele count: 1
allele frequency: 8.456230550669733e-6
allele num: 118256
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2338-36T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2248-36T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2068-36T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2326-36T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2080-36T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1477-36T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2080-36T>C
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8164
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23367
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3475
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7846
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1912
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

11-129785792-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785792
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785792
    reference: chr 11
allele count: 1
allele frequency: 8.4774499830451e-6
allele num: 117960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2068-37G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2326-37G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2080-37G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2080-37G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2338-37G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2248-37G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1477-37G>A
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6992
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22851
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3457
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7762
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6317
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

11-129785793-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785793
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785793
    reference: chr 11
allele count: 1
allele frequency: 8.476012883539584e-6
allele num: 117980
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2248-38T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2326-38T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2080-38T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1477-38T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2068-38T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2080-38T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2338-38T>C
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1302
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22324
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2612
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

11-129785806-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129785806
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129785806
    reference: chr 11
allele count: 1
allele frequency: 9.152480322167307e-6
allele num: 109260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1477-51A>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2326-51A>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2338-51A>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2248-51A>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2080-51A>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2080-51A>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2068-51A>C
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9871
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8842
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4099
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4303
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4758
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4606
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2358
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1735
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2296
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

11-129786977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129786977
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129786977
    reference: chr 11
allele count: 1
allele frequency: 8.549346829902196e-6
allele num: 116968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2247+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2067+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1476+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2079+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2337+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2325+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2079+45C>T
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11465
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2417
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2199
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4032
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

11-129786979-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129786979
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129786979
    reference: chr 11
allele count: 1
allele frequency: 8.536939336509074e-6
allele num: 117138
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2337+43T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2247+43T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2079+43T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1476+43T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2067+43T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2325+43T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2079+43T>C
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 22610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28465
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4190
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3550
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

11-129786983-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129786983
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129786983
    reference: chr 11
allele count: 1
allele frequency: 8.508755509419192e-6
allele num: 117526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1476+39T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2067+39T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2325+39T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2337+39T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2079+39T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2247+39T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2079+39T>A
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1217
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2760
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD

11-129786986-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129786986
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129786986
    reference: chr 11
allele count: 23
allele frequency: 1.958046720697405e-4
allele num: 117464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2079+36G>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2325+36G>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2337+36G>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1476+36G>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2247+36G>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2067+36G>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2079+36G>C
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4200
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26616
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12817
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33972
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1928
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5194
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

11-129787001-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787001
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787001
    reference: chr 11
allele count: 1
allele frequency: 8.386588168201411e-6
allele num: 119238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2079+21T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2079+21T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2247+21T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1476+21T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2325+21T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2337+21T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2067+21T>C
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5667
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-129787027-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787027
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787027
    reference: chr 11
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2062G>A
  hgvsp: ENSP00000302669.6:p.Asp688Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2074G>A
  hgvsp: ENSP00000432237.1:p.Asp692Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2320G>A
  hgvsp: ENSP00000354118.3:p.Asp774Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1471G>A
  hgvsp: ENSP00000435940.1:p.Asp491Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2332G>A
  hgvsp: ENSP00000351686.5:p.Asp778Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2242G>A
  hgvsp: ENSP00000431262.1:p.Asp748Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2074G>A
  hgvsp: ENSP00000398431.2:p.Asp692Asn
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46357
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp778Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

11-129787028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787028
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787028
    reference: chr 11
allele count: 2
allele frequency: 1.652428243303535e-5
allele num: 121034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2073C>T
  hgvsp: ENST00000526082.1:c.2073C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2073C>T
  hgvsp: ENST00000423662.2:c.2073C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2319C>T
  hgvsp: ENST00000360871.3:c.2319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2331C>T
  hgvsp: ENST00000358825.5:c.2331C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1470C>T
  hgvsp: ENST00000533431.1:c.1470C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2061C>T
  hgvsp: ENST00000304538.6:c.2061C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2241C>T
  hgvsp: ENST00000528746.1:c.2241C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Cys777Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

11-129787031-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787031
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787031
    reference: chr 11
allele count: 3
allele frequency: 2.477373323644051e-5
allele num: 121096
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2328T>C
  hgvsp: ENST00000358825.5:c.2328T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2070T>C
  hgvsp: ENST00000526082.1:c.2070T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2070T>C
  hgvsp: ENST00000423662.2:c.2070T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2058T>C
  hgvsp: ENST00000304538.6:c.2058T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2316T>C
  hgvsp: ENST00000360871.3:c.2316T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1467T>C
  hgvsp: ENST00000533431.1:c.1467T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2238T>C
  hgvsp: ENST00000528746.1:c.2238T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr776Tyr
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: A
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

11-129787067-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787067
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787067
    reference: chr 11
allele count: 3
allele frequency: 2.472717681579902e-5
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1431C>T
  hgvsp: ENST00000533431.1:c.1431C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2280C>T
  hgvsp: ENST00000360871.3:c.2280C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2022C>T
  hgvsp: ENST00000304538.6:c.2022C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2034C>T
  hgvsp: ENST00000526082.1:c.2034C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2292C>T
  hgvsp: ENST00000358825.5:c.2292C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2202C>T
  hgvsp: ENST00000528746.1:c.2202C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2034C>T
  hgvsp: ENST00000423662.2:c.2034C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5931
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro764Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

11-129787070-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787070
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787070
    reference: chr 11
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2289A>T
  hgvsp: ENST00000358825.5:c.2289A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2277A>T
  hgvsp: ENST00000360871.3:c.2277A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2199A>T
  hgvsp: ENST00000528746.1:c.2199A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1428A>T
  hgvsp: ENST00000533431.1:c.1428A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2031A>T
  hgvsp: ENST00000423662.2:c.2031A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2031A>T
  hgvsp: ENST00000526082.1:c.2031A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2019A>T
  hgvsp: ENST00000304538.6:c.2019A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46794
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  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: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu763Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS

11-129787073-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787073
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787073
    reference: chr 11
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2274T>A
  hgvsp: ENST00000360871.3:c.2274T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2028T>A
  hgvsp: ENST00000526082.1:c.2028T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2016T>A
  hgvsp: ENST00000304538.6:c.2016T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1425T>A
  hgvsp: ENST00000533431.1:c.1425T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2286T>A
  hgvsp: ENST00000358825.5:c.2286T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2196T>A
  hgvsp: ENST00000528746.1:c.2196T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2028T>A
  hgvsp: ENST00000423662.2:c.2028T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  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: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  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: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46806
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr762Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

11-129787074-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787074
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787074
    reference: chr 11
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2027C>A
  hgvsp: ENSP00000432237.1:p.Thr676Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2285C>A
  hgvsp: ENSP00000351686.5:p.Thr762Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2027C>A
  hgvsp: ENSP00000398431.2:p.Thr676Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2195C>A
  hgvsp: ENSP00000431262.1:p.Thr732Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2273C>A
  hgvsp: ENSP00000354118.3:p.Thr758Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1424C>A
  hgvsp: ENSP00000435940.1:p.Thr475Asn
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.2015C>A
  hgvsp: ENSP00000302669.6:p.Thr672Asn
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46787
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr762Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

11-129787097-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787097
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787097
    reference: chr 11
allele count: 2
allele frequency: 1.649974425396406e-5
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.2004G>A
  hgvsp: ENST00000526082.1:c.2004G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1401G>A
  hgvsp: ENST00000533431.1:c.1401G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.2004G>A
  hgvsp: ENST00000423662.2:c.2004G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2250G>A
  hgvsp: ENST00000360871.3:c.2250G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1992G>A
  hgvsp: ENST00000304538.6:c.1992G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2172G>A
  hgvsp: ENST00000528746.1:c.2172G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2262G>A
  hgvsp: ENST00000358825.5:c.2262G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5911
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys754Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-129787102-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787102
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787102
    reference: chr 11
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2167A>G
  hgvsp: ENSP00000431262.1:p.Met723Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1999A>G
  hgvsp: ENSP00000432237.1:p.Met667Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1987A>G
  hgvsp: ENSP00000302669.6:p.Met663Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2257A>G
  hgvsp: ENSP00000351686.5:p.Met753Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1396A>G
  hgvsp: ENSP00000435940.1:p.Met466Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2245A>G
  hgvsp: ENSP00000354118.3:p.Met749Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1999A>G
  hgvsp: ENSP00000398431.2:p.Met667Val
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46522
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met753Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

11-129787115-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787115
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787115
    reference: chr 11
allele count: 1
allele frequency: 8.278145695364238e-6
allele num: 120800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1383G>A
  hgvsp: ENST00000533431.1:c.1383G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2154G>A
  hgvsp: ENST00000528746.1:c.2154G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1986G>A
  hgvsp: ENST00000526082.1:c.1986G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1974G>A
  hgvsp: ENST00000304538.6:c.1974G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2244G>A
  hgvsp: ENST00000358825.5:c.2244G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2232G>A
  hgvsp: ENST00000360871.3:c.2232G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1986G>A
  hgvsp: ENST00000423662.2:c.1986G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33318
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4180
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46020
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5869
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys748Lys
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

11-129787127-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787127
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787127
    reference: chr 11
allele count: 4
allele frequency: 3.344313830409846e-5
allele num: 119606
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2232T>C
  hgvsp: ENST00000358825.5:c.2232T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1974T>C
  hgvsp: ENST00000526082.1:c.1974T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2220T>C
  hgvsp: ENST00000360871.3:c.2220T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1974T>C
  hgvsp: ENST00000423662.2:c.1974T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1962T>C
  hgvsp: ENST00000304538.6:c.1962T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2142T>C
  hgvsp: ENST00000528746.1:c.2142T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1371T>C
  hgvsp: ENST00000533431.1:c.1371T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5766
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43909
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1189
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4181
  bin: 9.75e1
  variant carriers: 4
hgvs: p.Asn744Asn
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

11-129787138-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787138
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787138
    reference: chr 11
allele count: 25
allele frequency: 2.132341652308899e-4
allele num: 117242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1969-6C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1957-6C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2137-6C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1969-6C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2227-6C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1366-6C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2215-6C>G
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27500
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16439
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5490
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39446
  bin: 6.25e1
  variant carriers: 0
hgvs: c.2227-6C>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

11-129787163-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787163
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787163
    reference: chr 11
allele count: 1
allele frequency: 9.077045966160773e-6
allele num: 110168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2215-31T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1969-31T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2137-31T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2227-31T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1957-31T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1366-31T>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1969-31T>A
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11568
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17547
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4564
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6830
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

11-129787165-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787165
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787165
    reference: chr 11
allele count: 2
allele frequency: 1.820830298616169e-5
allele num: 109840
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1957-33C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1366-33C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2137-33C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2215-33C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2227-33C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1969-33C>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1969-33C>G
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16908
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10605
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16823
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

11-129787173-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129787173
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129787173
    reference: chr 11
allele count: 9
allele frequency: 8.375988832014891e-5
allele num: 107450
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2227-41T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1969-41T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2137-41T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2215-41T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1969-41T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1957-41T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1366-41T>C
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16792
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15625
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6237
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2157
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2568
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8323
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2456
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

11-129788389-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788389
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788389
    reference: chr 11
allele count: 2
allele frequency: 1.692648826148039e-5
allele num: 118158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+45C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+45C>T
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1263
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46590
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

11-129788396-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788396
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788396
    reference: chr 11
allele count: 1
allele frequency: 8.4530853761623e-6
allele num: 118300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+38A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+38A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+38A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+38A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+38A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+38A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+38A>G
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2834
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-129788398-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788398
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788398
    reference: chr 11
allele count: 11
allele frequency: 9.294151443973165e-5
allele num: 118354
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+36C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+36C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+36C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+36C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+36C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+36C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+36C>T
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1175
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46595
  bin: 9.75e1
  variant carriers: 11
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP

11-129788407-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788407
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788407
    reference: chr 11
allele count: 8
allele frequency: 6.737182510274203e-5
allele num: 118744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+27T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+27T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+27T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+27T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+27T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+27T>C
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+27T>C
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3380
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-129788412-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788412
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788412
    reference: chr 11
allele count: 1
allele frequency: 8.412551526878102e-6
allele num: 118870
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+22G>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+22G>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+22G>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+22G>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+22G>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+22G>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+22G>T
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6136
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3722
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46597
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
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: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

11-129788412-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788412
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788412
    reference: chr 11
allele count: 1
allele frequency: 8.412551526878102e-6
allele num: 118870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+22G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+22G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+22G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+22G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+22G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+22G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+22G>A
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46597
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3722
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

11-129788413-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788413
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788413
    reference: chr 11
allele count: 2
allele frequency: 1.681067814275628e-5
allele num: 118972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+21G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+21G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+21G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+21G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+21G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+21G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+21G>A
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3869
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-129788414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788414
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788414
    reference: chr 11
allele count: 1
allele frequency: 8.402514032198434e-6
allele num: 119012
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+20G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+20G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+20G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+20G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+20G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+20G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+20G>A
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3944
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

11-129788415-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788415
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788415
    reference: chr 11
allele count: 11
allele frequency: 9.233455326864318e-5
allele num: 119132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+19C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+19C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+19C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+19C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+19C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+19C>T
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+19C>T
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46605
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

11-129788416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788416
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788416
    reference: chr 11
allele count: 3
allele frequency: 2.516736296370866e-5
allele num: 119202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+18G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+18G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+18G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+18G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+18G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+18G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+18G>A
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46603
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4260
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

11-129788422-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788422
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788422
    reference: chr 11
allele count: 1
allele frequency: 8.352125615969264e-6
allele num: 119730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+12G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+12G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+12G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+12G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+12G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+12G>A
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+12G>A
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-129788423-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788423
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788423
    reference: chr 11
allele count: 3
allele frequency: 2.504048211274894e-5
allele num: 119806
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+11A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+11A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+11A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+11A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+11A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+11A>G
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+11A>G
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5052
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

11-129788423-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788423
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788422
    reference: chr 11
allele count: 1
allele frequency: 8.346827370916315e-6
allele num: 119806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1365+10delC
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2226+10delC
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1968+10delC
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2136+10delC
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2214+10delC
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1968+10delC
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1956+10delC
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1627
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46604
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: TG
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

11-129788442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788442
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788442
    reference: chr 11
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1960G>A
  hgvsp: ENSP00000398431.2:p.Gly654Ser
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2206G>A
  hgvsp: ENSP00000354118.3:p.Gly736Ser
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1960G>A
  hgvsp: ENSP00000432237.1:p.Gly654Ser
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2128G>A
  hgvsp: ENSP00000431262.1:p.Gly710Ser
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2218G>A
  hgvsp: ENSP00000351686.5:p.Gly740Ser
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1357G>A
  hgvsp: ENSP00000435940.1:p.Gly453Ser
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1948G>A
  hgvsp: ENSP00000302669.6:p.Gly650Ser
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46604
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly740Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

11-129788443-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788443
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788443
    reference: chr 11
allele count: 1
allele frequency: 8.272940865018697e-6
allele num: 120876
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2217C>T
  hgvsp: ENST00000358825.5:c.2217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1959C>T
  hgvsp: ENST00000526082.1:c.1959C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2205C>T
  hgvsp: ENST00000360871.3:c.2205C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1947C>T
  hgvsp: ENST00000304538.6:c.1947C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1959C>T
  hgvsp: ENST00000423662.2:c.1959C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1356C>T
  hgvsp: ENST00000533431.1:c.1356C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2127C>T
  hgvsp: ENST00000528746.1:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg739Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

11-129788450-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788450
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788450
    reference: chr 11
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2210G>A
  hgvsp: ENSP00000351686.5:p.Arg737Gln
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1349G>A
  hgvsp: ENSP00000435940.1:p.Arg450Gln
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2120G>A
  hgvsp: ENSP00000431262.1:p.Arg707Gln
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1952G>A
  hgvsp: ENSP00000432237.1:p.Arg651Gln
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1952G>A
  hgvsp: ENSP00000398431.2:p.Arg651Gln
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2198G>A
  hgvsp: ENSP00000354118.3:p.Arg733Gln
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1940G>A
  hgvsp: ENSP00000302669.6:p.Arg647Gln
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6617
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg737Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

11-129788451-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788451
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788451
    reference: chr 11
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1939C>T
  hgvsp: ENSP00000302669.6:p.Arg647Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1951C>T
  hgvsp: ENSP00000398431.2:p.Arg651Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2209C>T
  hgvsp: ENSP00000351686.5:p.Arg737Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1951C>T
  hgvsp: ENSP00000432237.1:p.Arg651Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2197C>T
  hgvsp: ENSP00000354118.3:p.Arg733Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2119C>T
  hgvsp: ENSP00000431262.1:p.Arg707Trp
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1348C>T
  hgvsp: ENSP00000435940.1:p.Arg450Trp
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46606
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg737Trp
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

11-129788461-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788461
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788461
    reference: chr 11
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2199G>A
  hgvsp: ENSP00000351686.5:p.Met733Ile
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1941G>A
  hgvsp: ENSP00000432237.1:p.Met647Ile
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2109G>A
  hgvsp: ENSP00000431262.1:p.Met703Ile
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1338G>A
  hgvsp: ENSP00000435940.1:p.Met446Ile
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1929G>A
  hgvsp: ENSP00000302669.6:p.Met643Ile
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2187G>A
  hgvsp: ENSP00000354118.3:p.Met729Ile
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1941G>A
  hgvsp: ENSP00000398431.2:p.Met647Ile
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1628
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met733Ile
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

11-129788463-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788463
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788463
    reference: chr 11
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2197A>G
  hgvsp: ENSP00000351686.5:p.Met733Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2185A>G
  hgvsp: ENSP00000354118.3:p.Met729Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2107A>G
  hgvsp: ENSP00000431262.1:p.Met703Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1336A>G
  hgvsp: ENSP00000435940.1:p.Met446Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1927A>G
  hgvsp: ENSP00000302669.6:p.Met643Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1939A>G
  hgvsp: ENSP00000432237.1:p.Met647Val
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1939A>G
  hgvsp: ENSP00000398431.2:p.Met647Val
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1510
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  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
hgvs: p.Met733Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-129788467-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788467
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788467
    reference: chr 11
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1332G>A
  hgvsp: ENST00000533431.1:c.1332G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1935G>A
  hgvsp: ENST00000526082.1:c.1935G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2103G>A
  hgvsp: ENST00000528746.1:c.2103G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1935G>A
  hgvsp: ENST00000423662.2:c.1935G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2181G>A
  hgvsp: ENST00000360871.3:c.2181G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2193G>A
  hgvsp: ENST00000358825.5:c.2193G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1923G>A
  hgvsp: ENST00000304538.6:c.1923G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu731Leu
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

11-129788469-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788469
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788469
    reference: chr 11
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1933C>T
  hgvsp: ENST00000526082.1:c.1933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2179C>T
  hgvsp: ENST00000360871.3:c.2179C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1921C>T
  hgvsp: ENST00000304538.6:c.1921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1330C>T
  hgvsp: ENST00000533431.1:c.1330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2191C>T
  hgvsp: ENST00000358825.5:c.2191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2101C>T
  hgvsp: ENST00000528746.1:c.2101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1933C>T
  hgvsp: ENST00000423662.2:c.1933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6901
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu731Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

11-129788482-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788482
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788482
    reference: chr 11
allele count: 5
allele frequency: 4.119023297195769e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2178G>A
  hgvsp: ENST00000358825.5:c.2178G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2166G>A
  hgvsp: ENST00000360871.3:c.2166G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1317G>A
  hgvsp: ENST00000533431.1:c.1317G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1920G>A
  hgvsp: ENST00000526082.1:c.1920G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1920G>A
  hgvsp: ENST00000423662.2:c.1920G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2088G>A
  hgvsp: ENST00000528746.1:c.2088G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1908G>A
  hgvsp: ENST00000304538.6:c.1908G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46608
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr726Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

11-129788494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788494
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788494
    reference: chr 11
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2076C>T
  hgvsp: ENST00000528746.1:c.2076C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1896C>T
  hgvsp: ENST00000304538.6:c.1896C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2154C>T
  hgvsp: ENST00000360871.3:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1908C>T
  hgvsp: ENST00000526082.1:c.1908C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1908C>T
  hgvsp: ENST00000423662.2:c.1908C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2166C>T
  hgvsp: ENST00000358825.5:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1305C>T
  hgvsp: ENST00000533431.1:c.1305C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46606
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr722Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-129788500-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788500
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788500
    reference: chr 11
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1890A>G
  hgvsp: ENST00000304538.6:c.1890A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2148A>G
  hgvsp: ENST00000360871.3:c.2148A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2160A>G
  hgvsp: ENST00000358825.5:c.2160A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1902A>G
  hgvsp: ENST00000526082.1:c.1902A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1299A>G
  hgvsp: ENST00000533431.1:c.1299A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1902A>G
  hgvsp: ENST00000423662.2:c.1902A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2070A>G
  hgvsp: ENST00000528746.1:c.2070A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46606
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.75e1
  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: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr720Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

11-129788506-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788506
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788506
    reference: chr 11
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1896G>A
  hgvsp: ENST00000526082.1:c.1896G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1293G>A
  hgvsp: ENST00000533431.1:c.1293G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2142G>A
  hgvsp: ENST00000360871.3:c.2142G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2064G>A
  hgvsp: ENST00000528746.1:c.2064G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1884G>A
  hgvsp: ENST00000304538.6:c.1884G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2154G>A
  hgvsp: ENST00000358825.5:c.2154G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1896G>A
  hgvsp: ENST00000423662.2:c.1896G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  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: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr718Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-129788507-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788507
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788507
    reference: chr 11
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1895C>T
  hgvsp: ENSP00000432237.1:p.Thr632Met
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1895C>T
  hgvsp: ENSP00000398431.2:p.Thr632Met
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1292C>T
  hgvsp: ENSP00000435940.1:p.Thr431Met
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2141C>T
  hgvsp: ENSP00000354118.3:p.Thr714Met
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2063C>T
  hgvsp: ENSP00000431262.1:p.Thr688Met
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1883C>T
  hgvsp: ENSP00000302669.6:p.Thr628Met
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2153C>T
  hgvsp: ENSP00000351686.5:p.Thr718Met
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6964
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr718Met
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-129788513-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788513
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788513
    reference: chr 11
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1286G>A
  hgvsp: ENSP00000435940.1:p.Arg429His
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1889G>A
  hgvsp: ENSP00000432237.1:p.Arg630His
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2057G>A
  hgvsp: ENSP00000431262.1:p.Arg686His
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2135G>A
  hgvsp: ENSP00000354118.3:p.Arg712His
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2147G>A
  hgvsp: ENSP00000351686.5:p.Arg716His
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1889G>A
  hgvsp: ENSP00000398431.2:p.Arg630His
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1877G>A
  hgvsp: ENSP00000302669.6:p.Arg626His
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  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: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46607
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg716His
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum

11-129788517-GCTTGAACGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788517
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788508
    reference: chr 11
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsp: ENSP00000354118.3:p.Thr708_Lys710del
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsp: ENSP00000431262.1:p.Thr682_Lys684del
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsp: ENSP00000398431.2:p.Thr626_Lys628del
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsp: ENSP00000302669.6:p.Thr622_Lys624del
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsp: ENSP00000432237.1:p.Thr626_Lys628del
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsp: ENSP00000351686.5:p.Thr712_Lys714del
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsp: ENSP00000435940.1:p.Thr425_Lys427del
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  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: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46607
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr712_Lys714del
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: GCTTGAACGT
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

11-129788521-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 129788521
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 129788521
    reference: chr 11
allele count: 26
allele frequency: 2.141645112930594e-4
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000431262
  ensembl transcript: ENST00000528746
  gene symbol: PRDM10
  hgvsc: ENST00000528746.1:c.2049C>G
  hgvsp: ENSP00000431262.1:p.Phe683Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000398431
  ensembl transcript: ENST00000423662
  gene symbol: PRDM10
  hgvsc: ENST00000423662.2:c.1881C>G
  hgvsp: ENSP00000398431.2:p.Phe627Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000351686
  ensembl transcript: ENST00000358825
  gene symbol: PRDM10
  hgvsc: ENST00000358825.5:c.2139C>G
  hgvsp: ENSP00000351686.5:p.Phe713Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000435940
  ensembl transcript: ENST00000533431
  gene symbol: PRDM10
  hgvsc: ENST00000533431.1:c.1278C>G
  hgvsp: ENSP00000435940.1:p.Phe426Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000354118
  ensembl transcript: ENST00000360871
  gene symbol: PRDM10
  hgvsc: ENST00000360871.3:c.2127C>G
  hgvsp: ENSP00000354118.3:p.Phe709Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000302669
  ensembl transcript: ENST00000304538
  gene symbol: PRDM10
  hgvsc: ENST00000304538.6:c.1869C>G
  hgvsp: ENSP00000302669.6:p.Phe623Leu
  variant of: http://identifiers.org/hgnc/13995
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170325
  ensembl protein: ENSP00000432237
  ensembl transcript: ENST00000526082
  gene symbol: PRDM10
  hgvsc: ENST00000526082.1:c.1881C>G
  hgvsp: ENSP00000432237.1:p.Phe627Leu
  variant of: http://identifiers.org/hgnc/13995
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe713Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G

South Asian
type: Population
allele count: 0
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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FS
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DP
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MQRankSum
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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Other
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European (Finnish)
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South Asian
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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FS
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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DP
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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African
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Other
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European (Finnish)
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South Asian
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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Other
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East Asian
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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QD
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MQRankSum
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BaseQRankSum
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DP
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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East Asian
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ClippingRankSum
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MQ
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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DP
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QD
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African
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Latino
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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FS
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MQ
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DP
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BaseQRankSum
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MQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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Other
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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QD
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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DP
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African
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Latino
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South Asian
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East Asian
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European (Non-Finnish)
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MQRankSum
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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QD
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BaseQRankSum
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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VQSLOD
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DP
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African
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South Asian
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European (Non-Finnish)
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FS
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Finnish)
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East Asian
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South Asian
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FS
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ReadPosRankSum
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VQSLOD
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SIO_000300: -2.527e-1

QD
type: SiteQuality
SIO_000300: 1.118e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.038e0

DP
type: SiteQuality
SIO_000300: 2.279126e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.603e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.237e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 8.53e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 2.278818e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2727
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.581e0

QD
type: SiteQuality
SIO_000300: 8.300000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 5.988e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.353e0

DP
type: SiteQuality
SIO_000300: 2.277373e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

VQSLOD
type: SiteQuality
SIO_000300: -1.036e0

FS
type: SiteQuality
SIO_000300: 3.756e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 218
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 107
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507386192342478e-5
allele num: 66340
num of homozygotes: 0

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15800
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.671e0

VQSLOD
type: SiteQuality
SIO_000300: -1.406e0

MQRankSum
type: SiteQuality
SIO_000300: 2.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.244224e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.782e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

QD
type: SiteQuality
SIO_000300: 1.107e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507977199384745e-5
allele num: 66314
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: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.412e0

VQSLOD
type: SiteQuality
SIO_000300: -1.896e0

MQ
type: SiteQuality
SIO_000300: 5.767e1

DP
type: SiteQuality
SIO_000300: 2.236596e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e0

QD
type: SiteQuality
SIO_000300: 1.436e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66208
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.35e0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.804e1

QD
type: SiteQuality
SIO_000300: 1.141e1

DP
type: SiteQuality
SIO_000300: 2.222222e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510984859931704e-5
allele num: 66182
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.436663233779608e-5
allele num: 15536
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: 11544
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.677e0

DP
type: SiteQuality
SIO_000300: 2.215661e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.575e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.78e-2

QD
type: SiteQuality
SIO_000300: 2.823e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.464124111182935e-5
allele num: 15470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66154
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.137e1

DP
type: SiteQuality
SIO_000300: 2.210239e6

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.58e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.94e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.176193836744295e-4
allele num: 8502
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65670
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

DP
type: SiteQuality
SIO_000300: 2.133485e6

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.889e1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525180733916969e-5
allele num: 65566
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.127564e6

MQRankSum
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.464e0

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

African
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: 65558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.177024482109228e-4
allele num: 8496
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

DP
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SIO_000300: 2.120745e6

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11138
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61352
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.238850346878097e-4
allele num: 8072
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.989324e6

BaseQRankSum
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ClippingRankSum
type: SiteQuality
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FS
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
type: SiteQuality
SIO_000300: -3.535e0

QD
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SIO_000300: 8.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.588e0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6504
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10106
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Latino
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allele count: 1
allele frequency: 8.941344778254649e-5
allele num: 11184
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64200
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.372e0

MQRankSum
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SIO_000300: 8.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
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SIO_000300: 1.336e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

DP
type: SiteQuality
SIO_000300: 1.570608e6

QD
type: SiteQuality
SIO_000300: 1.49e1

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

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

South Asian
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allele count: 1
allele frequency: 6.372673973999491e-5
allele num: 15692
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64304
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11210
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.384e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.68e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

VQSLOD
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DP
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SIO_000300: 1.584916e6

BaseQRankSum
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SIO_000300: -5.448e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.25e-1

QD
type: SiteQuality
SIO_000300: 1.236e1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15758
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549618793776731e-5
allele num: 64532
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.48e-1

DP
type: SiteQuality
SIO_000300: 1.604409e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.09e-1

QD
type: SiteQuality
SIO_000300: 1.011e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

South Asian
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allele count: 6
allele frequency: 3.812913065582105e-4
allele num: 15736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.1441647597254e-3
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.662406815761449e-4
allele num: 11268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.016191569217408e-4
allele num: 64478
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.31e0

VQSLOD
type: SiteQuality
SIO_000300: 5.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
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MQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.622636e6

QD
type: SiteQuality
SIO_000300: 1.366e1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.164686699277894e-4
allele num: 8586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
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: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65542
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15992
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InbreedingCoeff
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SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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QD
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66532
num of homozygotes: 0

South Asian
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African
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Other
type: Population
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DP
type: SiteQuality
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BaseQRankSum
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FS
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MQRankSum
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.005530175522962e-5
allele num: 66544
num of homozygotes: 0

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

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

FS
type: SiteQuality
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MQ
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ReadPosRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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South Asian
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African
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allele frequency: 2.892960462873674e-4
allele num: 10370
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European (Finnish)
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Latino
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Other
type: Population
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QD
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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DP
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99868058054456e-5
allele num: 66696
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.038e0

QD
type: SiteQuality
SIO_000300: 1.06e1

MQ
type: SiteQuality
SIO_000300: 5.919e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.649e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.92e-1

DP
type: SiteQuality
SIO_000300: 1.760774e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-1

GenotypeQuality
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variant carriers: 0

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

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: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.760628e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.68e-1

QD
type: SiteQuality
SIO_000300: 5.92e0

MQ
type: SiteQuality
SIO_000300: 5.886e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.97e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.11e0

FS
type: SiteQuality
SIO_000300: 1.431e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.631e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.026e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.760752e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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: 0
allele frequency: 0.0e0
allele num: 11560
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: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.760693e6

VQSLOD
type: SiteQuality
SIO_000300: 6.41e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
SIO_000300: 5.533e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.052e0

MQRankSum
type: SiteQuality
SIO_000300: 6.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-1

QD
type: SiteQuality
SIO_000300: 1.212e1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 46688
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GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
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: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 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: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 1.759523e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.856999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.64e-1

QD
type: SiteQuality
SIO_000300: 1.139e1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

GenotypeQuality
all individuals: 1214
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 612
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
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: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

FS
type: SiteQuality
SIO_000300: 5.674e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.791e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.149e-1

QD
type: SiteQuality
SIO_000300: 1.006e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.758108e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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: 10354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66390
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.217e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 1.753236e6

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.229709788489916e-4
allele num: 16264
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.343566908835247e-4
allele num: 8534
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65648
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.521e1

FS
type: SiteQuality
SIO_000300: 1.766e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.73191e6

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 9
allele frequency: 1.404275237946637e-4
allele num: 64090
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11198
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 15
allele frequency: 9.334163036714375e-4
allele num: 16070
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Other
type: Population
allele count: 1
allele frequency: 1.128668171557562e-3
allele num: 886
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MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.685196e6

FS
type: SiteQuality
SIO_000300: 9.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.676e0

QD
type: SiteQuality
SIO_000300: 1.477e1

VQSLOD
type: SiteQuality
SIO_000300: 3.06e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 494
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.680502806439687e-5
allele num: 59506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7634
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.193e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.575e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.027e0

DP
type: SiteQuality
SIO_000300: 1.417573e6

QD
type: SiteQuality
SIO_000300: 1.916e1

GenotypeQuality
all individuals: 4170
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 264
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2853
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variant carriers: 0

GenotypeQuality
all individuals: 4888
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.371998920960345e-5
allele num: 59312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.083e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.36e0

QD
type: SiteQuality
SIO_000300: 1.486e1

MQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.79e-1

DP
type: SiteQuality
SIO_000300: 1.406257e6

GenotypeQuality
all individuals: 5145
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.541326067211626e-4
allele num: 15414
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.731361889262094e-5
allele num: 57758
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6188
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.748488984207447e-5
allele num: 10258
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

FS
type: SiteQuality
SIO_000300: 3.03e0

DP
type: SiteQuality
SIO_000300: 1.346895e6

QD
type: SiteQuality
SIO_000300: 1.378e1

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2291
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variant carriers: 0

GenotypeQuality
all individuals: 130
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 1109
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65694
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.313208420078649e-4
allele num: 8646
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.342e0

FS
type: SiteQuality
SIO_000300: 4.237e0

VQSLOD
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 3.383918e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.707e0

QD
type: SiteQuality
SIO_000300: 1.359e1

GenotypeQuality
all individuals: 642
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variant carriers: 0

GenotypeQuality
all individuals: 44
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1110
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14506
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65744
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: -1.427e-1

DP
type: SiteQuality
SIO_000300: 3.388373e6

QD
type: SiteQuality
SIO_000300: 1.554e1

MQRankSum
type: SiteQuality
SIO_000300: -6.3e-2

FS
type: SiteQuality
SIO_000300: 1.762e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.373e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 143
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1452
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GenotypeQuality
all individuals: 131
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GenotypeQuality
all individuals: 260
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GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 1100
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variant carriers: 0

GenotypeQuality
all individuals: 637
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variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.024803387779795e-4
allele num: 6612
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.040943789035392e-3
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14552
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.287e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

MQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

QD
type: SiteQuality
SIO_000300: 1.426e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 3.389688e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1215
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 46597
bin: 9.75e1
variant carriers: 8

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.250693802035153e-4
allele num: 8648
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65862
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.945e1

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.45e-1

DP
type: SiteQuality
SIO_000300: 3.397313e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 9.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

QD
type: SiteQuality
SIO_000300: 1.552e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 60
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14888
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: 11554
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.674e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.349e1

MQ
type: SiteQuality
SIO_000300: 5.927e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.851e0

DP
type: SiteQuality
SIO_000300: 3.401548e6

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14888
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65908
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
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.927e1

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312673450508788e-4
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65930
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: 11554
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.402942e6

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.091e0

QD
type: SiteQuality
SIO_000300: 1.28e1

MQ
type: SiteQuality
SIO_000300: 5.928e1

VQSLOD
type: SiteQuality
SIO_000300: 3.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 159
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GenotypeQuality
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GenotypeQuality
all individuals: 1253
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1276
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GenotypeQuality
all individuals: 480
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GenotypeQuality
all individuals: 46596
bin: 9.75e1
variant carriers: 1

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: 14994
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
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: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516576177621402e-5
allele num: 65938
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.693e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.32e-1

DP
type: SiteQuality
SIO_000300: 3.404734e6

QD
type: SiteQuality
SIO_000300: 2.098e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4127
bin: 6.25e1
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GenotypeQuality
all individuals: 1626
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1130
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.971337579617834e-4
allele num: 15072
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515840533575868e-5
allele num: 65970
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: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

DP
type: SiteQuality
SIO_000300: 3.406887e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.49e0

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.367e1

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 424
bin: 2.75e1
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GenotypeQuality
all individuals: 86
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 1626
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65998
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15116
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: 3
allele frequency: 2.887947631882942e-4
allele num: 10388
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.422e0

DP
type: SiteQuality
SIO_000300: 3.408738e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

VQSLOD
type: SiteQuality
SIO_000300: -3.634e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

FS
type: SiteQuality
SIO_000300: 9.574e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.336e1

MQRankSum
type: SiteQuality
SIO_000300: 7.89e-1

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
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variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
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: 884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511441613010489e-5
allele num: 66162
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: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15464
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.984e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.28e0

DP
type: SiteQuality
SIO_000300: 3.417606e6

FS
type: SiteQuality
SIO_000300: 1.291e0

MQRankSum
type: SiteQuality
SIO_000300: -1.152e0

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-2

QD
type: SiteQuality
SIO_000300: 1.14e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.243e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
all individuals: 1154
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 298
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variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 8.75e1
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: 11562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15516
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66182
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.885725278953444e-4
allele num: 10396
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.57e-1

QD
type: SiteQuality
SIO_000300: 1.241e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 3.418866e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

FS
type: SiteQuality
SIO_000300: 4.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5052
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
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variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
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: 1
allele frequency: 1.510984859931704e-5
allele num: 66182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15516
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 4.2e0

QD
type: SiteQuality
SIO_000300: 1.241e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQRankSum
type: SiteQuality
SIO_000300: -3.57e-1

DP
type: SiteQuality
SIO_000300: 3.418866e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.07e-1

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 120
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 400
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variant carriers: 0

GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 1
allele frequency: 1.504528631179851e-5
allele num: 66466
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: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16124
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.436047e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.202e0

VQSLOD
type: SiteQuality
SIO_000300: -1.084e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.538e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e0

MQRankSum
type: SiteQuality
SIO_000300: 2.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.503e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 1627
bin: 9.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1155
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GenotypeQuality
all individuals: 1442
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16230
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66500
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.421e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.33e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.167e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.88e0

FS
type: SiteQuality
SIO_000300: 9.618e0

DP
type: SiteQuality
SIO_000300: 3.438003e6

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 871
bin: 8.75e1
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: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 1.502042778178322e-5
allele num: 66576
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.443476e6

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.84e-2

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 1.482e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1285
bin: 8.25e1
variant carriers: 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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501817198810561e-5
allele num: 66586
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -9.916e-1

MQ
type: SiteQuality
SIO_000300: 5.921e1

FS
type: SiteQuality
SIO_000300: 3.023e0

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.652e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.55e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.34e0

DP
type: SiteQuality
SIO_000300: 3.444105e6

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

Latino
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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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16500
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

DP
type: SiteQuality
SIO_000300: 3.446735e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: -8.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.773e0

FS
type: SiteQuality
SIO_000300: 3.749e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-2

QD
type: SiteQuality
SIO_000300: 1.345e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.98e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e-1

GenotypeQuality
all individuals: 9
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variant carriers: 0

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

European (Finnish)
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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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

FS
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SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.61e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.38e-1

BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 3.446604e6

MQ
type: SiteQuality
SIO_000300: 5.986e1

MQRankSum
type: SiteQuality
SIO_000300: -7.23e-1

QD
type: SiteQuality
SIO_000300: 1.169e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.319e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

GenotypeQuality
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variant carriers: 0

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

Other
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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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

MQRankSum
type: SiteQuality
SIO_000300: 5.49e-1

DP
type: SiteQuality
SIO_000300: 3.447136e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.37e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.765e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.37e-2

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: 5.3e-2

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.998770504093322e-5
allele num: 66694
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
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VQSLOD
type: SiteQuality
SIO_000300: -4.526e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.44759e6

MQ
type: SiteQuality
SIO_000300: 5.991e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

QD
type: SiteQuality
SIO_000300: 1.377e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 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

MQ
type: SiteQuality
SIO_000300: 5.988e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.05e-2

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.788e0

DP
type: SiteQuality
SIO_000300: 3.44857e6

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
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
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

FS
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

MQRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -8.92e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele num: 16512
num of homozygotes: 0

East Asian
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allele count: 0
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allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
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num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.35e-1

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.65e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

Other
type: Population
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

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

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: 1.498486528606108e-5
allele num: 66734
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: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.448155e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.176e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.386e0

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

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

GenotypeQuality
all individuals: 1518
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6962
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1284
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.448202e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQRankSum
type: SiteQuality
SIO_000300: -9.93e0

VQSLOD
type: SiteQuality
SIO_000300: 1.83e-1

FS
type: SiteQuality
SIO_000300: 2.987e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.799e0

MQ
type: SiteQuality
SIO_000300: 5.327e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.04e-1

QD
type: SiteQuality
SIO_000300: 4.41e0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6960
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46606
bin: 9.75e1
variant carriers: 26

GenotypeQuality
all individuals: 1284
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 672
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 0
bin: 4.75e1
variant carriers: 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: 26
allele frequency: 3.896298516409411e-4
allele num: 66730
num of homozygotes: 0

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

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

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

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