http://identifiers.org/exac.variant/8-42037432-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037432
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037432
    reference: chr 8
allele count: 1
allele frequency: 1.314682372738746e-5
allele num: 76064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.985+12G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1225+12G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1096+12G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1363+12G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.855+12G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1174+12G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1363+12G>T
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13587
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2029
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1768
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22880
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4720
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-42037433-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037433
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037433
    reference: chr 8
allele count: 1
allele frequency: 1.309346112551392e-5
allele num: 76374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.985+11G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1096+11G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.855+11G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1225+11G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1363+11G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1363+11G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1174+11G>A
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17031
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17211
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

8-42037444-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037444
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037444
    reference: chr 8
allele count: 14
allele frequency: 1.76246947151094e-4
allele num: 79434
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1363T>C
  hgvsp: ENST00000429089.2:c.1363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.855T>C
  hgvsp: ENST00000270189.6:c.855T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1363T>C
  hgvsp: ENST00000220809.4:c.1363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.985T>C
  hgvsp: ENST00000429710.2:c.985T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1174T>C
  hgvsp: ENST00000519510.1:c.1174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1096T>C
  hgvsp: ENST00000524009.1:c.1096T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1225T>C
  hgvsp: ENST00000352041.3:c.1225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13077
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19351
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4436
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 5.75e1
  variant carriers: 0
hgvs: c.1363T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum

http://identifiers.org/exac.variant/8-42037447-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037447
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037447
    reference: chr 8
allele count: 9
allele frequency: 1.121663052419053e-4
allele num: 80238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1222G>T
  hgvsp: ENSP00000270188.6:p.Ala408Ser
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1360G>T
  hgvsp: ENSP00000392045.2:p.Ala454Ser
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.852G>T
  hgvsp: ENSP00000270189.6:p.Arg284Ser
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1171G>T
  hgvsp: ENSP00000428886.1:p.Ala391Ser
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.982G>T
  hgvsp: ENSP00000407861.2:p.Ala328Ser
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1360G>T
  hgvsp: ENSP00000220809.4:p.Ala454Ser
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1093G>T
  hgvsp: ENSP00000429401.1:p.Ala365Ser
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17737
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13328
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22538
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4496
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18256
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala454Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

8-42037448-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037448
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037448
    reference: chr 8
allele count: 7
allele frequency: 8.706034525645491e-5
allele num: 80404
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1359G>C
  hgvsp: ENSP00000220809.4:p.Glu453Asp
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1359G>C
  hgvsp: ENSP00000392045.2:p.Glu453Asp
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1170G>C
  hgvsp: ENSP00000428886.1:p.Glu390Asp
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1221G>C
  hgvsp: ENSP00000270188.6:p.Glu407Asp
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.851G>C
  hgvsp: ENSP00000270189.6:p.Arg284Thr
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1092G>C
  hgvsp: ENSP00000429401.1:p.Glu364Asp
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.981G>C
  hgvsp: ENSP00000407861.2:p.Glu327Asp
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13452
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4589
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17497
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2036
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu453Asp
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS

8-42037448-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037448
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037448
    reference: chr 8
allele count: 2
allele frequency: 2.487438435898711e-5
allele num: 80404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.851G>A
  hgvsp: ENSP00000270189.6:p.Arg284Lys
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1359G>A
  hgvsp: ENST00000429089.2:c.1359G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1170G>A
  hgvsp: ENST00000519510.1:c.1170G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1221G>A
  hgvsp: ENST00000352041.3:c.1221G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1092G>A
  hgvsp: ENST00000524009.1:c.1092G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.981G>A
  hgvsp: ENST00000429710.2:c.981G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1359G>A
  hgvsp: ENST00000220809.4:c.1359G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4552
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg284Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-42037466-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037466
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037466
    reference: chr 8
allele count: 2
allele frequency: 2.361609673153221e-5
allele num: 84688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1341C>T
  hgvsp: ENST00000429089.2:c.1341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1152C>T
  hgvsp: ENST00000519510.1:c.1152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.833C>T
  hgvsp: ENSP00000270189.6:p.Pro278Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1341C>T
  hgvsp: ENST00000220809.4:c.1341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1203C>T
  hgvsp: ENST00000352041.3:c.1203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1074C>T
  hgvsp: ENST00000524009.1:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.963C>T
  hgvsp: ENST00000429710.2:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15347
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6287
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14910
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2791
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5171
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro278Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

8-42037479-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037479
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037479
    reference: chr 8
allele count: 10
allele frequency: 1.156042634852373e-4
allele num: 86502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.950A>C
  hgvsp: ENSP00000407861.2:p.Glu317Ala
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1139A>C
  hgvsp: ENSP00000428886.1:p.Glu380Ala
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.820A>C
  hgvsp: ENSP00000270189.6:p.Ser274Arg
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1328A>C
  hgvsp: ENSP00000392045.2:p.Glu443Ala
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1190A>C
  hgvsp: ENSP00000270188.6:p.Glu397Ala
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1328A>C
  hgvsp: ENSP00000220809.4:p.Glu443Ala
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1061A>C
  hgvsp: ENSP00000429401.1:p.Glu354Ala
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12982
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8362
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16273
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3639
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5747
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1316
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20144
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5881
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu443Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

8-42037487-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037487
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037487
    reference: chr 8
allele count: 1
allele frequency: 1.132425882725976e-5
allele num: 88306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1182C>T
  hgvsp: ENST00000352041.3:c.1182C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1131C>T
  hgvsp: ENST00000519510.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1053C>T
  hgvsp: ENST00000524009.1:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1320C>T
  hgvsp: ENST00000429089.2:c.1320C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.812C>T
  hgvsp: ENSP00000270189.6:p.Thr271Ile
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1320C>T
  hgvsp: ENST00000220809.4:c.1320C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.942C>T
  hgvsp: ENST00000429710.2:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13966
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3602
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5812
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1439
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1242
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr271Ile
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

8-42037489-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037489
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037489
    reference: chr 8
allele count: 2
allele frequency: 2.262443438914027e-5
allele num: 88400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1180G>C
  hgvsp: ENSP00000270188.6:p.Asp394His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1318G>C
  hgvsp: ENSP00000392045.2:p.Asp440His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1051G>C
  hgvsp: ENSP00000429401.1:p.Asp351His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.810G>C
  hgvsp: ENST00000270189.6:c.810G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.940G>C
  hgvsp: ENSP00000407861.2:p.Asp314His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1129G>C
  hgvsp: ENSP00000428886.1:p.Asp377His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1318G>C
  hgvsp: ENSP00000220809.4:p.Asp440His
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8250
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3700
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20297
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp440His
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

8-42037489-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037489
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037489
    reference: chr 8
allele count: 1
allele frequency: 1.131221719457014e-5
allele num: 88400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.940G>A
  hgvsp: ENSP00000407861.2:p.Asp314Asn
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1129G>A
  hgvsp: ENSP00000428886.1:p.Asp377Asn
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1318G>A
  hgvsp: ENSP00000220809.4:p.Asp440Asn
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1318G>A
  hgvsp: ENSP00000392045.2:p.Asp440Asn
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1051G>A
  hgvsp: ENSP00000429401.1:p.Asp351Asn
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.810G>A
  hgvsp: ENST00000270189.6:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1180G>A
  hgvsp: ENSP00000270188.6:p.Asp394Asn
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16328
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20297
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp440Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-42037490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037490
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037490
    reference: chr 8
allele count: 1
allele frequency: 1.130582249858677e-5
allele num: 88450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1179G>A
  hgvsp: ENST00000352041.3:c.1179G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.809G>A
  hgvsp: ENSP00000270189.6:p.Arg270Gln
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.939G>A
  hgvsp: ENST00000429710.2:c.939G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1317G>A
  hgvsp: ENST00000220809.4:c.1317G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1317G>A
  hgvsp: ENST00000429089.2:c.1317G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1050G>A
  hgvsp: ENST00000524009.1:c.1050G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1128G>A
  hgvsp: ENST00000519510.1:c.1128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1429
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1236
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5833
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20344
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5645
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14737
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg270Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

8-42037492-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037492
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037492
    reference: chr 8
allele count: 2
allele frequency: 2.257387299939051e-5
allele num: 88598
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1315C>G
  hgvsp: ENSP00000220809.4:p.Pro439Ala
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.937C>G
  hgvsp: ENSP00000407861.2:p.Pro313Ala
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1126C>G
  hgvsp: ENSP00000428886.1:p.Pro376Ala
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1315C>G
  hgvsp: ENSP00000392045.2:p.Pro439Ala
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1048C>G
  hgvsp: ENSP00000429401.1:p.Pro350Ala
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.807C>G
  hgvsp: ENSP00000270189.6:p.Cys269Trp
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1177C>G
  hgvsp: ENSP00000270188.6:p.Pro393Ala
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8440
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14929
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5739
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5908
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1306
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3730
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro439Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

8-42037506-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037506
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037506
    reference: chr 8
allele count: 1
allele frequency: 1.105607641960021e-5
allele num: 90448
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1034C>T
  hgvsp: ENSP00000429401.1:p.Ala345Val
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-11C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1163C>T
  hgvsp: ENSP00000270188.6:p.Ala388Val
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1112C>T
  hgvsp: ENSP00000428886.1:p.Ala371Val
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1301C>T
  hgvsp: ENSP00000220809.4:p.Ala434Val
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.923C>T
  hgvsp: ENSP00000407861.2:p.Ala308Val
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1301C>T
  hgvsp: ENSP00000392045.2:p.Ala434Val
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14144
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3817
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ala434Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ

8-42037506-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037506
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037506
    reference: chr 8
allele count: 2
allele frequency: 2.211215283920042e-5
allele num: 90448
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1112C>A
  hgvsp: ENSP00000428886.1:p.Ala371Glu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1301C>A
  hgvsp: ENSP00000220809.4:p.Ala434Glu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1034C>A
  hgvsp: ENSP00000429401.1:p.Ala345Glu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1301C>A
  hgvsp: ENSP00000392045.2:p.Ala434Glu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1163C>A
  hgvsp: ENSP00000270188.6:p.Ala388Glu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.923C>A
  hgvsp: ENSP00000407861.2:p.Ala308Glu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-11C>A
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8583
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16478
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14144
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5798
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala434Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

8-42037508-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037508
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037508
    reference: chr 8
allele count: 4
allele frequency: 4.412381141483001e-5
allele num: 90654
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1299G>A
  hgvsp: ENST00000220809.4:c.1299G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.921G>A
  hgvsp: ENST00000429710.2:c.921G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1299G>A
  hgvsp: ENST00000429089.2:c.1299G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1161G>A
  hgvsp: ENST00000352041.3:c.1161G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1110G>A
  hgvsp: ENST00000519510.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1032G>A
  hgvsp: ENST00000524009.1:c.1032G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-13G>A
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8441
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16334
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14472
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5724
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19423
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5940
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro433Pro
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

8-42037511-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037511
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037511
    reference: chr 8
allele count: 2
allele frequency: 2.176894442388489e-5
allele num: 91874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-16C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.918C>T
  hgvsp: ENST00000429710.2:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1296C>T
  hgvsp: ENST00000220809.4:c.1296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1296C>T
  hgvsp: ENST00000429089.2:c.1296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1107C>T
  hgvsp: ENST00000519510.1:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1029C>T
  hgvsp: ENST00000524009.1:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1158C>T
  hgvsp: ENST00000352041.3:c.1158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16107
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7962
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5535
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro432Pro
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

8-42037511-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037511
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037511
    reference: chr 8
allele count: 4
allele frequency: 4.353788884776977e-5
allele num: 91874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1029C>A
  hgvsp: ENST00000524009.1:c.1029C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.918C>A
  hgvsp: ENST00000429710.2:c.918C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1107C>A
  hgvsp: ENST00000519510.1:c.1107C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1158C>A
  hgvsp: ENST00000352041.3:c.1158C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1296C>A
  hgvsp: ENST00000220809.4:c.1296C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-16C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1296C>A
  hgvsp: ENST00000429089.2:c.1296C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16107
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7962
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15387
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5770
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19459
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro432Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD

8-42037520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037520
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037520
    reference: chr 8
allele count: 5
allele frequency: 5.359746162421748e-5
allele num: 93288
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1287G>A
  hgvsp: ENST00000220809.4:c.1287G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.909G>A
  hgvsp: ENST00000429710.2:c.909G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-25G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1149G>A
  hgvsp: ENST00000352041.3:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1098G>A
  hgvsp: ENST00000519510.1:c.1098G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1287G>A
  hgvsp: ENST00000429089.2:c.1287G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1020G>A
  hgvsp: ENST00000524009.1:c.1020G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15740
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16052
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5423
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3550
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val429Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum

8-42037527-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037527
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037527
    reference: chr 8
allele count: 3
allele frequency: 3.218262567315325e-5
allele num: 93218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1142G>A
  hgvsp: ENSP00000270188.6:p.Arg381His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-32G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1280G>A
  hgvsp: ENSP00000220809.4:p.Arg427His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1091G>A
  hgvsp: ENSP00000428886.1:p.Arg364His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1013G>A
  hgvsp: ENSP00000429401.1:p.Arg338His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.902G>A
  hgvsp: ENSP00000407861.2:p.Arg301His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1280G>A
  hgvsp: ENSP00000392045.2:p.Arg427His
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8514
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16233
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5361
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1541
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18017
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3599
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg427His
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

http://identifiers.org/exac.variant/8-42037532-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037532
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037532
    reference: chr 8
allele count: 1
allele frequency: 1.050817536043042e-5
allele num: 95164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1137G>T
  hgvsp: ENST00000352041.3:c.1137G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-37G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1086G>T
  hgvsp: ENST00000519510.1:c.1086G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1275G>T
  hgvsp: ENST00000429089.2:c.1275G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1008G>T
  hgvsp: ENST00000524009.1:c.1008G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1275G>T
  hgvsp: ENST00000220809.4:c.1275G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.897G>T
  hgvsp: ENST00000429710.2:c.897G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15329
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3595
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1663
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val425Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

8-42037532-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037532
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037532
    reference: chr 8
allele count: 1
allele frequency: 1.050817536043042e-5
allele num: 95164
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1275G>A
  hgvsp: ENST00000220809.4:c.1275G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1086G>A
  hgvsp: ENST00000519510.1:c.1086G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-37G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1137G>A
  hgvsp: ENST00000352041.3:c.1137G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.897G>A
  hgvsp: ENST00000429710.2:c.897G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1275G>A
  hgvsp: ENST00000429089.2:c.1275G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1008G>A
  hgvsp: ENST00000524009.1:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15329
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1369
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17645
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val425Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/8-42037533-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037533
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037533
    reference: chr 8
allele count: 2
allele frequency: 2.093057328840237e-5
allele num: 95554
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1274T>G
  hgvsp: ENSP00000392045.2:p.Val425Gly
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1136T>G
  hgvsp: ENSP00000270188.6:p.Val379Gly
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1007T>G
  hgvsp: ENSP00000429401.1:p.Val336Gly
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1085T>G
  hgvsp: ENSP00000428886.1:p.Val362Gly
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1274T>G
  hgvsp: ENSP00000220809.4:p.Val425Gly
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.896T>G
  hgvsp: ENSP00000407861.2:p.Val299Gly
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-38T>G
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15248
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5164
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17728
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5533
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17589
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val425Gly
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/8-42037534-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037534
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037534
    reference: chr 8
allele count: 1
allele frequency: 1.047976357653371e-5
allele num: 95422
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1084G>T
  hgvsp: ENSP00000428886.1:p.Val362Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1273G>T
  hgvsp: ENSP00000220809.4:p.Val425Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1273G>T
  hgvsp: ENSP00000392045.2:p.Val425Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.895G>T
  hgvsp: ENSP00000407861.2:p.Val299Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1135G>T
  hgvsp: ENSP00000270188.6:p.Val379Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.1006G>T
  hgvsp: ENSP00000429401.1:p.Val336Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-39G>T
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8055
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17221
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5140
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17422
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5528
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val425Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-42037541-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037541
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037541
    reference: chr 8
allele count: 2
allele frequency: 2.06011413032282e-5
allele num: 97082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.888G>C
  hgvsp: ENSP00000407861.2:p.Glu296Asp
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-46G>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.999G>C
  hgvsp: ENSP00000429401.1:p.Glu333Asp
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1128G>C
  hgvsp: ENSP00000270188.6:p.Glu376Asp
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1077G>C
  hgvsp: ENSP00000428886.1:p.Glu359Asp
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1266G>C
  hgvsp: ENSP00000220809.4:p.Glu422Asp
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1266G>C
  hgvsp: ENSP00000392045.2:p.Glu422Asp
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14359
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19108
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16722
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19651
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu422Asp
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

8-42037549-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037549
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037549
    reference: chr 8
allele count: 1
allele frequency: 1.016033000751864e-5
allele num: 98422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1069G>A
  hgvsp: ENSP00000428886.1:p.Ala357Thr
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1120G>A
  hgvsp: ENSP00000270188.6:p.Ala374Thr
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-54G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1258G>A
  hgvsp: ENSP00000220809.4:p.Ala420Thr
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.991G>A
  hgvsp: ENSP00000429401.1:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1258G>A
  hgvsp: ENSP00000392045.2:p.Ala420Thr
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.880G>A
  hgvsp: ENSP00000407861.2:p.Ala294Thr
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4633
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5053
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3358
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1317
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala420Thr
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD

8-42037552-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037552
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037552
    reference: chr 8
allele count: 1
allele frequency: 1.007252215954875e-5
allele num: 99280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1255T>C
  hgvsp: ENSP00000392045.2:p.Cys419Arg
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.877T>C
  hgvsp: ENSP00000407861.2:p.Cys293Arg
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-57T>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1255T>C
  hgvsp: ENSP00000220809.4:p.Cys419Arg
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1066T>C
  hgvsp: ENSP00000428886.1:p.Cys356Arg
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1117T>C
  hgvsp: ENSP00000270188.6:p.Cys373Arg
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.988T>C
  hgvsp: ENSP00000429401.1:p.Cys330Arg
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20218
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15718
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1602
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4976
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Cys419Arg
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: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

8-42037553-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037553
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037553
    reference: chr 8
allele count: 1
allele frequency: 1.006765463917526e-5
allele num: 99328
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1254C>T
  hgvsp: ENST00000220809.4:c.1254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1254C>T
  hgvsp: ENST00000429089.2:c.1254C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1065C>T
  hgvsp: ENST00000519510.1:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.987C>T
  hgvsp: ENST00000524009.1:c.987C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1116C>T
  hgvsp: ENST00000352041.3:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.876C>T
  hgvsp: ENST00000429710.2:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-58C>T
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3256
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4485
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20624
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4915
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg418Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

8-42037554-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037554
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037554
    reference: chr 8
allele count: 1
allele frequency: 1.011204141892165e-5
allele num: 98892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-59G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1253G>A
  hgvsp: ENSP00000220809.4:p.Arg418His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1064G>A
  hgvsp: ENSP00000428886.1:p.Arg355His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1253G>A
  hgvsp: ENSP00000392045.2:p.Arg418His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.875G>A
  hgvsp: ENSP00000407861.2:p.Arg292His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1115G>A
  hgvsp: ENSP00000270188.6:p.Arg372His
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.986G>A
  hgvsp: ENSP00000429401.1:p.Arg329His
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20244
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4880
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15359
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3307
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg418His
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

8-42037555-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037555
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037555
    reference: chr 8
allele count: 3
allele frequency: 3.008121929208864e-5
allele num: 99730
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1252C>T
  hgvsp: ENSP00000220809.4:p.Arg418Cys
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.874C>T
  hgvsp: ENSP00000407861.2:p.Arg292Cys
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1252C>T
  hgvsp: ENSP00000392045.2:p.Arg418Cys
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1114C>T
  hgvsp: ENSP00000270188.6:p.Arg372Cys
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1063C>T
  hgvsp: ENSP00000428886.1:p.Arg355Cys
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-60C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.985C>T
  hgvsp: ENSP00000429401.1:p.Arg329Cys
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20674
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9945
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15173
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4384
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4744
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg418Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

8-42037555-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037555
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037555
    reference: chr 8
allele count: 1
allele frequency: 1.002707309736288e-5
allele num: 99730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1252C>A
  hgvsp: ENSP00000392045.2:p.Arg418Ser
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.985C>A
  hgvsp: ENSP00000429401.1:p.Arg329Ser
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-60C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1114C>A
  hgvsp: ENSP00000270188.6:p.Arg372Ser
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1063C>A
  hgvsp: ENSP00000428886.1:p.Arg355Ser
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.874C>A
  hgvsp: ENSP00000407861.2:p.Arg292Ser
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1252C>A
  hgvsp: ENSP00000220809.4:p.Arg418Ser
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13141
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9945
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3228
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4384
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15173
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg418Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

8-42037559-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037559
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037559
    reference: chr 8
allele count: 1
allele frequency: 9.940357852882704e-6
allele num: 100600
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1248G>C
  hgvsp: ENST00000429089.2:c.1248G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1110G>C
  hgvsp: ENST00000352041.3:c.1110G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.981G>C
  hgvsp: ENST00000524009.1:c.981G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1059G>C
  hgvsp: ENST00000519510.1:c.1059G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1248G>C
  hgvsp: ENST00000220809.4:c.1248G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.870G>C
  hgvsp: ENST00000429710.2:c.870G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-64G>C
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4216
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21731
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4624
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser416Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

8-42037566-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037566
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037566
    reference: chr 8
allele count: 2
allele frequency: 1.953277599812485e-5
allele num: 102392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1052C>T
  hgvsp: ENSP00000428886.1:p.Ser351Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.863C>T
  hgvsp: ENSP00000407861.2:p.Ser288Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1103C>T
  hgvsp: ENSP00000270188.6:p.Ser368Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.974C>T
  hgvsp: ENSP00000429401.1:p.Ser325Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1241C>T
  hgvsp: ENSP00000220809.4:p.Ser414Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1241C>T
  hgvsp: ENSP00000392045.2:p.Ser414Leu
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-71C>T
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7362
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11689
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1170
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1216
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3214
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2806
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser414Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

8-42037568-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037568
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037568
    reference: chr 8
allele count: 1
allele frequency: 9.700450100884681e-6
allele num: 103088
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1101A>G
  hgvsp: ENST00000352041.3:c.1101A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1239A>G
  hgvsp: ENST00000429089.2:c.1239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1050A>G
  hgvsp: ENST00000519510.1:c.1050A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1239A>G
  hgvsp: ENST00000220809.4:c.1239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.861A>G
  hgvsp: ENST00000429710.2:c.861A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-73A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.972A>G
  hgvsp: ENST00000524009.1:c.972A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13412
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24707
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3342
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3806
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys413Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/8-42037578-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037578
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037578
    reference: chr 8
allele count: 1
allele frequency: 9.525623928367308e-6
allele num: 104980
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.851T>G
  hgvsp: ENSP00000407861.2:p.Leu284Arg
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1229T>G
  hgvsp: ENSP00000392045.2:p.Leu410Arg
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1091T>G
  hgvsp: ENSP00000270188.6:p.Leu364Arg
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1040T>G
  hgvsp: ENSP00000428886.1:p.Leu347Arg
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1229T>G
  hgvsp: ENSP00000220809.4:p.Leu410Arg
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-83T>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.962T>G
  hgvsp: ENSP00000429401.1:p.Leu321Arg
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12184
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25083
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu410Arg
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum

8-42037579-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037579
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037579
    reference: chr 8
allele count: 1
allele frequency: 9.521089212605923e-6
allele num: 105030
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-84C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.961C>G
  hgvsp: ENSP00000429401.1:p.Leu321Val
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1228C>G
  hgvsp: ENSP00000220809.4:p.Leu410Val
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.850C>G
  hgvsp: ENSP00000407861.2:p.Leu284Val
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1039C>G
  hgvsp: ENSP00000428886.1:p.Leu347Val
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1090C>G
  hgvsp: ENSP00000270188.6:p.Leu364Val
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1228C>G
  hgvsp: ENSP00000392045.2:p.Leu410Val
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3465
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1881
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2532
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu410Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

8-42037582-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037582
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037582
    reference: chr 8
allele count: 1
allele frequency: 9.47633758505013e-6
allele num: 105526
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1225C>A
  hgvsp: ENSP00000220809.4:p.Leu409Met
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1087C>A
  hgvsp: ENSP00000270188.6:p.Leu363Met
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1225C>A
  hgvsp: ENSP00000392045.2:p.Leu409Met
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-87C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.958C>A
  hgvsp: ENSP00000429401.1:p.Leu320Met
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.847C>A
  hgvsp: ENSP00000407861.2:p.Leu283Met
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1036C>A
  hgvsp: ENSP00000428886.1:p.Leu346Met
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9922
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3667
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25019
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3306
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu409Met
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

8-42037583-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037583
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037583
    reference: chr 8
allele count: 1
allele frequency: 9.486046026295319e-6
allele num: 105418
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.957G>C
  hgvsp: ENST00000524009.1:c.957G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1035G>C
  hgvsp: ENST00000519510.1:c.1035G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1086G>C
  hgvsp: ENST00000352041.3:c.1086G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.846G>C
  hgvsp: ENST00000429710.2:c.846G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1224G>C
  hgvsp: ENST00000429089.2:c.1224G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1224G>C
  hgvsp: ENST00000220809.4:c.1224G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-88G>C
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9172
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3225
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3592
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1224G>C
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

8-42037583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037583
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037583
    reference: chr 8
allele count: 3
allele frequency: 2.845813807888596e-5
allele num: 105418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.957G>A
  hgvsp: ENST00000524009.1:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1224G>A
  hgvsp: ENST00000220809.4:c.1224G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1086G>A
  hgvsp: ENST00000352041.3:c.1086G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1224G>A
  hgvsp: ENST00000429089.2:c.1224G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-88G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.846G>A
  hgvsp: ENST00000429710.2:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1035G>A
  hgvsp: ENST00000519510.1:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25309
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3225
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1311
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11436
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1224G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/8-42037585-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037585
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037585
    reference: chr 8
allele count: 1
allele frequency: 9.410701850143983e-6
allele num: 106262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-1G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-90G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-1G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-1G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-1G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-1G>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-1G>T
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26103
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10958
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4245
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 7.25e1
  variant carriers: 0
hgvs: c.1223-1G>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

8-42037590-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037590
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037590
    reference: chr 8
allele count: 1
allele frequency: 9.282120778955576e-6
allele num: 107734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-6T>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-6T>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-95T>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-6T>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-6T>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-6T>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-6T>C
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4195
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9626
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1223-6T>C
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

8-42037591-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037591
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037591
    reference: chr 8
allele count: 1
allele frequency: 9.244365559191673e-6
allele num: 108174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-7C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-96C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-7C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-7C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-7C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-7C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-7C>A
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7843
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2791
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29548
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1223-7C>A
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

8-42037597-AAGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037597
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037594
    reference: chr 8
allele count: 1
allele frequency: 9.124587112433163e-6
allele num: 109594
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-16_1223-14delCCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-105_804-103delCCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-16_1034-14delCCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-16_845-14delCCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-16_1223-14delCCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-16_956-14delCCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-16_1085-14delCCT
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1590
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8344
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2422
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: AAGG
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

8-42037603-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037603
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037603
    reference: chr 8
allele count: 4
allele frequency: 3.615328994938539e-5
allele num: 110640
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-19C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-19C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.569C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-19C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-19C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-19C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-19C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-108C>G
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29091
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7269
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2062
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2117
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1954
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

8-42037605-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037605
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037605
    reference: chr 8
allele count: 33
allele frequency: 2.986317237385072e-4
allele num: 110504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-21C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.567C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-21C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-21C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-110C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-21C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-21C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-21C>T
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 28853
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12167
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1421
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 9.75e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29424
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1886
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

8-42037607-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037607
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037607
    reference: chr 8
allele count: 1
allele frequency: 9.021362586605081e-6
allele num: 110848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.565C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-23C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-23C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-112C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-23C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-23C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-23C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-23C>T
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6673
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2251
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30813
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

8-42037609-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037609
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037609
    reference: chr 8
allele count: 1
allele frequency: 8.98876404494382e-6
allele num: 111250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-25C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-25C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-25C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-25C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-25C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-114C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.563C>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-25C>G
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1707
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2346
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2237
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

8-42037611-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037611
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037611
    reference: chr 8
allele count: 1
allele frequency: 8.950307890591436e-6
allele num: 111728
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-27A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.561A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-27A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-27A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-116A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-27A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-27A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-27A>G
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4737
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6181
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2424
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-42037612-GGCGTGAGGGCC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037612
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037601
    reference: chr 8
allele count: 2
allele frequency: 1.78782136088962e-5
allele num: 111868
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5766
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: GGCGTGAGGGCC
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-42037614-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037614
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037614
    reference: chr 8
allele count: 1
allele frequency: 8.944383821398544e-6
allele num: 111802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-30G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.558G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-119G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-30G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-30G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-30G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-30G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-30G>A
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

8-42037615-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037615
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037615
    reference: chr 8
allele count: 1
allele frequency: 8.888098835659053e-6
allele num: 112510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.557C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-31C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-31C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-120C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-31C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-31C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-31C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-31C>T
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6591
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 909
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

8-42037623-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037623
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037623
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 113050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-39G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-39G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-39G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-128G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-39G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-39G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-39G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.549G>A
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3967
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

8-42037624-G-GCGTCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037624
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037629
    reference: chr 8
allele count: 1
allele frequency: 8.832985902554499e-6
allele num: 113212
alternate allele: GCGTCC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-45_845-41dupGGACG
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.543_547dupGGACG
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-45_1223-41dupGGACG
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-45_1034-41dupGGACG
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-45_1223-41dupGGACG
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-134_804-130dupGGACG
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-45_956-41dupGGACG
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-45_1085-41dupGGACG
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14052
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29425
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2762
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1881
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-42037625-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037625
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037625
    reference: chr 8
allele count: 3
allele frequency: 2.65050447935257e-5
allele num: 113186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-41G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.547G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-41G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-41G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-41G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-41G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-130G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-41G>A
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14093
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29355
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33391
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2776
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7054
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

8-42037628-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037628
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037628
    reference: chr 8
allele count: 409
allele frequency: 3.600669072981776e-3
allele num: 113590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-44G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-44G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-133G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.544G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-44G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-44G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-44G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-44G>A
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6594
  bin: 3.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 29067
  bin: 2.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14205
  bin: 2.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 33507
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3339
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3198
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 7
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

8-42037630-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037630
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037630
    reference: chr 8
allele count: 14461
allele frequency: 1.268152799214256e-1
allele num: 114032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-46G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-46G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-46G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-46G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.542G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-46G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-135G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-46G>A
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.75e1
  variant carriers: 742
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 1.75e1
  variant carriers: 405
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 4.75e1
  variant carriers: 1594
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 4.25e1
  variant carriers: 1869
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.5e0
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 11978
  bin: 2.75e1
  variant carriers: 1147
genotype depth: GenotypeDepth
  all individuals: 22725
  bin: 2.25e1
  variant carriers: 582
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 3.75e1
  variant carriers: 2034
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.25e1
  variant carriers: 508
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 7.5e0
  variant carriers: 543
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 1.25e1
  variant carriers: 693
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 5.25e1
  variant carriers: 1214
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.75e1
  variant carriers: 303
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 3.25e1
  variant carriers: 1741
genotype quality: GenotypeQuality
  all individuals: 25517
  bin: 6.25e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 3.75e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 2269
  bin: 7.25e1
  variant carriers: 61
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 8.75e1
  variant carriers: 97
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 1.75e1
  variant carriers: 47
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 2.75e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 2571
  bin: 7.75e1
  variant carriers: 107
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 5.75e1
  variant carriers: 42
num of homozygotes: 1059
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

8-42037631-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037631
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037631
    reference: chr 8
allele count: 121
allele frequency: 1.060938185006576e-3
allele num: 114050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-47G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-47G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-136G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-47G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.541G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-47G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-47G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-47G>A
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22443
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11824
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6066
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25787
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

8-42037631-CGGGAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037631
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037626
    reference: chr 8
allele count: 1
allele frequency: 8.768084173608067e-6
allele num: 114050
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1223-52_1223-48delCTCCC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1034-52_1034-48delCTCCC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-141_804-137delCTCCC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1085-52_1085-48delCTCCC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.956-52_956-48delCTCCC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.536_540delCTCCC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.845-52_845-48delCTCCC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1223-52_1223-48delCTCCC
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22443
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25787
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1351
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2343
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: CGGGAG
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-42037710-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037710
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037710
    reference: chr 8
allele count: 1
allele frequency: 8.321821480285606e-6
allele num: 120166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-215C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+50C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+50C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+50C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+50C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.462C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+50C>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+50C>A
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42689
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-42037716-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037716
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037716
    reference: chr 8
allele count: 1
allele frequency: 8.32639467110741e-6
allele num: 120100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+44A>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+44A>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+44A>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+44A>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-221A>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+44A>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.456A>C
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+44A>C
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42689
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

8-42037721-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037721
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037721
    reference: chr 8
allele count: 1
allele frequency: 8.312966565248474e-6
allele num: 120294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.451C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+39C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+39C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+39C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+39C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+39C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-226C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+39C>T
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42689
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52368
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

8-42037740-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037740
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037740
    reference: chr 8
allele count: 1
allele frequency: 8.292974192264313e-6
allele num: 120584
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+20G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+20G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.432G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+20G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-245G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+20G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+20G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+20G>A
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42689
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3585
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

8-42037740-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037740
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037739
    reference: chr 8
allele count: 1
allele frequency: 8.292974192264313e-6
allele num: 120584
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-246delC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+19delC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+19delC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.431delC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+19delC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+19delC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+19delC
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+19delC
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42689
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: CG
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ

8-42037741-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037741
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037741
    reference: chr 8
allele count: 332
allele frequency: 2.751214014617896e-3
allele num: 120674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+19C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+19C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+19C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+19C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+19C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.431C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-246C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+19C>T
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42733
  bin: 9.75e1
  variant carriers: 314
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52376
  bin: 9.75e1
  variant carriers: 332
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3820
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

8-42037742-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037742
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037742
    reference: chr 8
allele count: 2
allele frequency: 1.656753756689143e-5
allele num: 120718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+18C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+18C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-247C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.430C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+18C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+18C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+18C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+18C>T
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42720
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3811
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

8-42037743-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037743
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037744
    reference: chr 8
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-249_804-248insA
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+16_844+17insA
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+16_1222+17insA
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+16_1033+17insA
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+16_1222+17insA
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.428_429insA
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+16_955+17insA
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+16_1084+17insA
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42720
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

8-42037744-A-AAAATTGGTTTTGTTATACGTCATTTCACTTACAGTTGCAGTTTCTAAGAACCTATTTTTTCCAGGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037744
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037810
    reference: chr 8
allele count: 1
allele frequency: 8.278145695364238e-6
allele num: 120800
alternate allele: AAAATTGGTTTTGTTATACGTCATTTCACTTACAGTTGCAGTTTCTAAGAACCTATTTTTTCCAGGC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42720
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52363
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

8-42037746-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037746
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037746
    reference: chr 8
allele count: 1
allele frequency: 8.275953389830508e-6
allele num: 120832
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+14A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+14A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+14A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-251A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+14A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.426A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+14A>G
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+14A>G
  variant of: http://identifiers.org/hgnc/9051
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42721
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

8-42037752-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037752
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037752
    reference: chr 8
allele count: 1
allele frequency: 8.259411599517651e-6
allele num: 121074
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+8C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+8C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+8C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+8C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+8C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+8C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-257C>T
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.420C>T
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42721
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1222+8C>T
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

8-42037753-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037753
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037753
    reference: chr 8
allele count: 1
allele frequency: 8.257774694875225e-6
allele num: 121098
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+7G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+7G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+7G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+7G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+7G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.419G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+7G>A
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-258G>A
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42721
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1222+7G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

8-42037757-T-TAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42037757
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 42037759
    reference: chr 8
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: TAG
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000429401
  ensembl transcript: ENST00000524009
  gene symbol: PLAT
  hgvsc: ENST00000524009.1:c.955+2_955+3insCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104368
  ensembl transcript: ENST00000522812
  gene symbol: PLAT
  hgvsc: ENST00000522812.1:n.414_415insCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000220809
  ensembl transcript: ENST00000220809
  gene symbol: PLAT
  hgvsc: ENST00000220809.4:c.1222+2_1222+3insCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000407861
  ensembl transcript: ENST00000429710
  gene symbol: PLAT
  hgvsc: ENST00000429710.2:c.844+2_844+3insCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270188
  ensembl transcript: ENST00000352041
  gene symbol: PLAT
  hgvsc: ENST00000352041.3:c.1084+2_1084+3insCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000392045
  ensembl transcript: ENST00000429089
  gene symbol: PLAT
  hgvsc: ENST00000429089.2:c.1222+2_1222+3insCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000428886
  ensembl transcript: ENST00000519510
  gene symbol: PLAT
  hgvsc: ENST00000519510.1:c.1033+2_1033+3insCT
  variant of: http://identifiers.org/hgnc/9051
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104368
  ensembl protein: ENSP00000270189
  ensembl transcript: ENST00000270189
  gene symbol: PLAT
  hgvsc: ENST00000270189.6:c.804-263_804-262insCT
  variant of: http://identifiers.org/hgnc/9051
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42721
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 8.25e1
  variant carriers: 0
hgvs: c.1222+2_1222+3insCT
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

8-42037762-A-G
type: Variant
location: Region
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: G
canonical: true
consequence: missense
filter: PASS
hgvs: p.Ile407Thr
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 17390
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4569
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7246
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.411631846414455e-4
allele num: 7084
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43490
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

QD
type: SiteQuality
SIO_000300: 7.57e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.91e0

DP
type: SiteQuality
SIO_000300: 8.97237e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.811e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.21e-1

GenotypeQuality
all individuals: 596
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4545
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22809
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 392
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4663
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.291055718475073e-5
allele num: 43648
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.322e1

VQSLOD
type: SiteQuality
SIO_000300: -1.293e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

FS
type: SiteQuality
SIO_000300: 1.971e0

MQ
type: SiteQuality
SIO_000300: 5.889e1

DP
type: SiteQuality
SIO_000300: 9.00095e5

MQRankSum
type: SiteQuality
SIO_000300: -2.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

GenotypeQuality
all individuals: 4449
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 597
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1469
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1880
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22638
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18622
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.886323268206039e-4
allele num: 45040
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8108
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.229407425620851e-4
allele num: 8134
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.133e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

QD
type: SiteQuality
SIO_000300: 1.011e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.30283e5

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

GenotypeQuality
all individuals: 1487
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1279
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4514
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 231
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 7.75e1
variant carriers: 2

South Asian
type: Population
allele count: 8
allele frequency: 9.622323791195574e-4
allele num: 8314
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7508
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.222493887530562e-4
allele num: 8180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45466
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3452
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.62e-1

QD
type: SiteQuality
SIO_000300: 1.036e1

DP
type: SiteQuality
SIO_000300: 9.33397e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.07e-1

FS
type: SiteQuality
SIO_000300: 6.014e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.209e0

GenotypeQuality
all individuals: 22443
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4552
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 409
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 5.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45462
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 8.278145695364238e-4
allele num: 8456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3472
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.7e0

DP
type: SiteQuality
SIO_000300: 9.33959e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.791e0

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 5.84e-1

GenotypeQuality
all individuals: 232
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22443
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4589
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2036
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 827
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17497
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45462
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.662406815761449e-4
allele num: 7512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6750
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.791e0

FS
type: SiteQuality
SIO_000300: 5.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

DP
type: SiteQuality
SIO_000300: 9.33959e5

QD
type: SiteQuality
SIO_000300: 1.22e1

GenotypeQuality
all individuals: 1465
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5176
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16173
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1218
bin: 7.5e0
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47112
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.872659176029963e-4
allele num: 10680
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

FS
type: SiteQuality
SIO_000300: 4.812e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.28e-1

QD
type: SiteQuality
SIO_000300: 9.33e0

VQSLOD
type: SiteQuality
SIO_000300: 5.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

DP
type: SiteQuality
SIO_000300: 9.44954e5

GenotypeQuality
all individuals: 779
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1322
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1328
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2057
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11392
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11916
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 2.09608451412761e-4
allele num: 47708
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.84e-1

FS
type: SiteQuality
SIO_000300: 2.726e0

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

DP
type: SiteQuality
SIO_000300: 9.3589e5

QD
type: SiteQuality
SIO_000300: 1.254e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 366
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1254
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20559
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 118
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5660
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.19161105815062e-4
allele num: 8392
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6854
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12528
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

DP
type: SiteQuality
SIO_000300: 9.48339e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.417e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

QD
type: SiteQuality
SIO_000300: 1.433e1

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5701
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13761
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5882
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7664
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.587049674654817e-4
allele num: 12602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3656
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

DP
type: SiteQuality
SIO_000300: 9.47605e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.572000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.612e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

QD
type: SiteQuality
SIO_000300: 5.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.22e-1

GenotypeQuality
all individuals: 1286
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5701
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3700
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13761
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5882
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.056005592335211e-5
allele num: 48638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7664
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3656
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

FS
type: SiteQuality
SIO_000300: 2.612e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

DP
type: SiteQuality
SIO_000300: 9.47605e5

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.572000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.22e-1

GenotypeQuality
all individuals: 116
bin: 9.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.886435331230284e-5
allele num: 12680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7678
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

FS
type: SiteQuality
SIO_000300: 2.6673e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 1.74e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.322e0

VQSLOD
type: SiteQuality
SIO_000300: -4.248e0

DP
type: SiteQuality
SIO_000300: 9.51204e5

GenotypeQuality
all individuals: 217
bin: 8.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 389
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variant carriers: 0

GenotypeQuality
all individuals: 13677
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.573811772112055e-4
allele num: 12708
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6816
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3658
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.49616e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-1

QD
type: SiteQuality
SIO_000300: 9.75e0

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: 19424
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7804
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.613826709304096e-5
allele num: 13134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6862
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

Latino
type: Population
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: 3820
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.783e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -9.86e-1

DP
type: SiteQuality
SIO_000300: 9.64702e5

QD
type: SiteQuality
SIO_000300: 6.78e0

VQSLOD
type: SiteQuality
SIO_000300: -2.008e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

GenotypeQuality
all individuals: 6017
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1055
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 13824
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variant carriers: 0

GenotypeQuality
all individuals: 3817
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13134
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.370791844476055e-4
allele num: 8436
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.903e1

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -9.86e-1

DP
type: SiteQuality
SIO_000300: 9.64702e5

FS
type: SiteQuality
SIO_000300: 5.783e0

VQSLOD
type: SiteQuality
SIO_000300: -2.008e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.17e-1

QD
type: SiteQuality
SIO_000300: 6.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

GenotypeQuality
all individuals: 544
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variant carriers: 0

GenotypeQuality
all individuals: 1048
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 427
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GenotypeQuality
all individuals: 1305
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13166
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3844
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.377006127808579e-4
allele num: 6854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.005374403401115e-5
allele num: 49866
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

QD
type: SiteQuality
SIO_000300: 2.441e1

DP
type: SiteQuality
SIO_000300: 9.71902e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 1.4177e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.623e-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: 682
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.527167045741723e-4
allele num: 7914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50576
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3914
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.724e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.8154e5

QD
type: SiteQuality
SIO_000300: 1.097e1

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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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6910
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.253605769230769e-4
allele num: 13312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.977222397975324e-5
allele num: 50576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3914
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

African
type: Population
allele count: 0
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allele num: 7914
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MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

DP
type: SiteQuality
SIO_000300: 9.8154e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.724e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.097e1

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 9.719306430293134e-5
allele num: 51444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
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South Asian
type: Population
allele count: 0
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allele num: 13486
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4016
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Other
type: Population
allele count: 0
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allele num: 694
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.616e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.157e0

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.95056e5

FS
type: SiteQuality
SIO_000300: 7.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.94e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8030
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.88259046435782e-5
allele num: 51512
num of homozygotes: 0

East Asian
type: Population
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South Asian
type: Population
allele count: 1
allele frequency: 7.422802850356295e-5
allele num: 13472
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Other
type: Population
allele count: 0
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allele num: 700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4026
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 1.293e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.3e-2

DP
type: SiteQuality
SIO_000300: 1.005923e6

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-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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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7024
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4190
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8756
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 7.326007326007326e-5
allele num: 13650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.78e-1

DP
type: SiteQuality
SIO_000300: 1.017458e6

QD
type: SiteQuality
SIO_000300: 1.004e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.899912604020215e-5
allele num: 52634
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8756
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 13650
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7024
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4190
num of homozygotes: 0

QD
type: SiteQuality
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DP
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MQRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.597e-1

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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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.783006733751986e-5
allele num: 52868
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13674
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4220
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 2.522e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -2.9e-3

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.020718e6

VQSLOD
type: SiteQuality
SIO_000300: -1.033e0

QD
type: SiteQuality
SIO_000300: 8.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e0

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13624
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52832
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7064
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.13947128532361e-4
allele num: 8776
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.110000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.403e1

FS
type: SiteQuality
SIO_000300: 1.515e0

DP
type: SiteQuality
SIO_000300: 1.022816e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-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: 2

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4372
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 53864
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 7.291818579553741e-5
allele num: 13714
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.12082492714638e-4
allele num: 8922
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.048525e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

QD
type: SiteQuality
SIO_000300: 2.634e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.29e-1

FS
type: SiteQuality
SIO_000300: 4.235e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.824684329610977e-5
allele num: 54804
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13542
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7252
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4498
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MQRankSum
type: SiteQuality
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ClippingRankSum
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QD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

South Asian
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allele frequency: 7.377895824110964e-5
allele num: 13554
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9140
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4572
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Other
type: Population
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allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 55330
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

MQRankSum
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ClippingRankSum
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DP
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7310
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.805640821927702e-5
allele num: 55382
num of homozygotes: 0

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

Other
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num of homozygotes: 0

VQSLOD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
type: SiteQuality
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MQRankSum
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FS
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QD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.8114629374683e-5
allele num: 55204
num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7270
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQRankSum
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QD
type: SiteQuality
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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MQ
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BaseQRankSum
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1260
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.096122337520481e-4
allele num: 7324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55668
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8670
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4604
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.06e-1

FS
type: SiteQuality
SIO_000300: 3.458e0

DP
type: SiteQuality
SIO_000300: 1.092206e6

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

GenotypeQuality
all individuals: 1602
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
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variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.390983000739098e-5
allele num: 13530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55668
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9186
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

DP
type: SiteQuality
SIO_000300: 1.092206e6

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-2

FS
type: SiteQuality
SIO_000300: 3.458e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.06e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.25e1
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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 430
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variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8756
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9286
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.776072747939756e-5
allele num: 56304
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.105476e6

QD
type: SiteQuality
SIO_000300: 6.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.282e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.418e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.055e0

GenotypeQuality
all individuals: 4257
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3920
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.741432153803288e-5
allele num: 57424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4910
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8954
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.053962900505902e-4
allele num: 9488
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.136714e6

FS
type: SiteQuality
SIO_000300: 4.124e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-1

GenotypeQuality
all individuals: 783
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 510
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 248
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variant carriers: 0

GenotypeQuality
all individuals: 2684
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variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4998
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7590
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.728488954955578e-5
allele num: 57854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 1.686e0

QD
type: SiteQuality
SIO_000300: 1.161e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

VQSLOD
type: SiteQuality
SIO_000300: 1.89e-1

DP
type: SiteQuality
SIO_000300: 1.146301e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 190
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2507
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5208
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7726
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.596475235490732e-5
allele num: 13164
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.515e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQRankSum
type: SiteQuality
SIO_000300: -3.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.346e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.158e0

MQ
type: SiteQuality
SIO_000300: 5.872e1

DP
type: SiteQuality
SIO_000300: 1.182861e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.094e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 7740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.635919364691509e-5
allele num: 13096
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.872e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.721e0

QD
type: SiteQuality
SIO_000300: 1.515e1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.18417e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.881e0

FS
type: SiteQuality
SIO_000300: 3.158e0

VQSLOD
type: SiteQuality
SIO_000300: -1.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13010
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.682368775235532e-5
allele num: 59440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5332
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.291e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.387e0

DP
type: SiteQuality
SIO_000300: 1.198149e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59358
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.072731173567904e-4
allele num: 9322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9916
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12948
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.187e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 8.090000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.93e-2

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.204889e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.676e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
all individuals: 1273
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.025413473174667e-4
allele num: 9916
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12948
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.090000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.93e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.204889e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.187e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.44e-1

QD
type: SiteQuality
SIO_000300: 1.676e1

GenotypeQuality
all individuals: 270
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3346
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 962
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27059
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12914
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.06224771616741e-4
allele num: 9414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5442
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59852
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.220202e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.645e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.627e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.181e1

GenotypeQuality
all individuals: 1582
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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
all individuals: 1608
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7948
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5614
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.765625000000001e-5
allele num: 10240
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12924
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0569e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.272e0

QD
type: SiteQuality
SIO_000300: 2.419e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.254343e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

VQSLOD
type: SiteQuality
SIO_000300: -2.317e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

GenotypeQuality
all individuals: 376
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9466
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.704968944099378e-5
allele num: 10304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7982
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60918
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.878e1

DP
type: SiteQuality
SIO_000300: 1.260333e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.445e0

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.447e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.763e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 1.0569e1

QD
type: SiteQuality
SIO_000300: 2.419e1

GenotypeQuality
all individuals: 1878
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2217
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
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variant carriers: 0

GenotypeQuality
all individuals: 5223
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
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variant carriers: 0

GenotypeQuality
all individuals: 30953
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.61980044058572e-5
allele num: 61736
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8068
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5860
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.25e-1

FS
type: SiteQuality
SIO_000300: 1.656e0

MQ
type: SiteQuality
SIO_000300: 5.648e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.78e-1

DP
type: SiteQuality
SIO_000300: 1.293033e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.122e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.503e1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

GenotypeQuality
all individuals: 993
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
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variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5592
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variant carriers: 0

GenotypeQuality
all individuals: 31049
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
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variant carriers: 0

GenotypeQuality
all individuals: 1398
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 9.75e1
variant carriers: 4

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5972
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.414368184733804e-5
allele num: 62360
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.321369e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.14e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.268e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.0e-1

FS
type: SiteQuality
SIO_000300: 1.267e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

VQSLOD
type: SiteQuality
SIO_000300: 6.11e-1

GenotypeQuality
all individuals: 1695
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1066
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
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variant carriers: 0

GenotypeQuality
all individuals: 6837
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 1410
bin: 5.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 8.25e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 33
allele frequency: 5.287614164396731e-4
allele num: 62410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10734
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.184e0

QD
type: SiteQuality
SIO_000300: 1.248e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.328361e6

GenotypeQuality
all individuals: 567
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1813
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5870
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variant carriers: 0

GenotypeQuality
all individuals: 93
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GenotypeQuality
all individuals: 2204
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6042
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.973210014351777e-5
allele num: 12542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8220
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.156e0

VQSLOD
type: SiteQuality
SIO_000300: -1.265e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

QD
type: SiteQuality
SIO_000300: 9.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.04e-1

MQ
type: SiteQuality
SIO_000300: 5.863e1

DP
type: SiteQuality
SIO_000300: 1.339729e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 333
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variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9916
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6100
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.593523918794021e-5
allele num: 62754
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12560
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.78e-1

FS
type: SiteQuality
SIO_000300: 2.545e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.342e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.13e0

QD
type: SiteQuality
SIO_000300: 3.328e1

MQ
type: SiteQuality
SIO_000300: 5.909e1

DP
type: SiteQuality
SIO_000300: 1.350983e6

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

GenotypeQuality
all individuals: 1383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 537
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GenotypeQuality
all individuals: 32902
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variant carriers: 0

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

GenotypeQuality
all individuals: 470
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 316
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10926
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.586697131251587e-5
allele num: 63024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9960
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.365134e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-1

QD
type: SiteQuality
SIO_000300: 1.367e1

VQSLOD
type: SiteQuality
SIO_000300: 5.04e-1

FS
type: SiteQuality
SIO_000300: 3.066e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.415e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.09e-1

GenotypeQuality
all individuals: 1619
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2369
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32899
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2485
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6240
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.168367023636018e-5
allele num: 63124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10960
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.387e1

MQRankSum
type: SiteQuality
SIO_000300: -2.641e0

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

DP
type: SiteQuality
SIO_000300: 1.37034e6

QD
type: SiteQuality
SIO_000300: 3.72e0

FS
type: SiteQuality
SIO_000300: 2.429e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.57e-1

GenotypeQuality
all individuals: 702
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5354
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32644
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 7.5e0
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9970
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.198753296571566e-4
allele num: 8342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10996
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6218
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.066e0

DP
type: SiteQuality
SIO_000300: 1.380036e6

FS
type: SiteQuality
SIO_000300: 1.754e0

QD
type: SiteQuality
SIO_000300: 7.89e0

MQRankSum
type: SiteQuality
SIO_000300: -1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.762e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.615e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2490
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 95
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2661
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11058
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12468
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.191043353978085e-4
allele num: 8396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6262
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 4.781e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.205e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

DP
type: SiteQuality
SIO_000300: 1.390845e6

GenotypeQuality
all individuals: 389
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2691
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variant carriers: 0

GenotypeQuality
all individuals: 1802
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33463
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 543
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variant carriers: 0

GenotypeQuality
all individuals: 6924
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63932
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.858e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.426311e6

VQSLOD
type: SiteQuality
SIO_000300: -2.947e0

QD
type: SiteQuality
SIO_000300: 2.69e0

GenotypeQuality
all individuals: 347
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3729
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7040
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3091
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33292
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64042
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.892050506846879e-5
allele num: 11246
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.519e0

MQ
type: SiteQuality
SIO_000300: 5.143e1

FS
type: SiteQuality
SIO_000300: 5.849e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.101e1

DP
type: SiteQuality
SIO_000300: 1.432395e6

MQRankSum
type: SiteQuality
SIO_000300: -4.105e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e0

GenotypeQuality
all individuals: 598
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3670
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 344
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3115
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10022
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175640724194686e-4
allele num: 8506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56137775973519e-5
allele num: 64046
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.884150675195451e-5
allele num: 11256
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12120
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.43713e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 9.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.135e0

VQSLOD
type: SiteQuality
SIO_000300: 6.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

FS
type: SiteQuality
SIO_000300: 3.637e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-1

QD
type: SiteQuality
SIO_000300: 1.398e1

GenotypeQuality
all individuals: 648
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 627
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1005
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7193
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1493
bin: 9.75e1
variant carriers: 398

GenotypeQuality
all individuals: 389
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2853
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1972
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 390
allele frequency: 3.886784931233805e-2
allele num: 10034
num of homozygotes: 7

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.667081518357188e-5
allele num: 64280
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.32579105532968e-3
allele num: 11314
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.207729468599034e-3
allele num: 828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12132
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

FS
type: SiteQuality
SIO_000300: 1.546e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.518e0

VQSLOD
type: SiteQuality
SIO_000300: 4.51e0

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

DP
type: SiteQuality
SIO_000300: 1.457846e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.99e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

QD
type: SiteQuality
SIO_000300: 1.371e1

GenotypeQuality
all individuals: 356
bin: 2.5e0
variant carriers: 10

GenotypeQuality
all individuals: 476
bin: 7.5e0
variant carriers: 18

GenotypeQuality
all individuals: 782
bin: 3.25e1
variant carriers: 37

GenotypeQuality
all individuals: 2433
bin: 2.25e1
variant carriers: 47

GenotypeQuality
all individuals: 391
bin: 4.75e1
variant carriers: 56

GenotypeQuality
all individuals: 349
bin: 1.25e1
variant carriers: 15

GenotypeQuality
all individuals: 14099
bin: 9.75e1
variant carriers: 12990

GenotypeQuality
all individuals: 613
bin: 9.25e1
variant carriers: 84

GenotypeQuality
all individuals: 1699
bin: 8.25e1
variant carriers: 119

GenotypeQuality
all individuals: 302
bin: 4.25e1
variant carriers: 27

GenotypeQuality
all individuals: 5623
bin: 6.75e1
variant carriers: 48

GenotypeQuality
all individuals: 386
bin: 5.25e1
variant carriers: 64

Latino
type: Population
allele count: 507
allele frequency: 4.470899470899471e-2
allele num: 11340
num of homozygotes: 12

European (Finnish)
type: Population
allele count: 1179
allele frequency: 1.817761332099908e-1
allele num: 6486
num of homozygotes: 111

Other
type: Population
allele count: 133
allele frequency: 1.598557692307692e-1
allele num: 832
num of homozygotes: 13

East Asian
type: Population
allele count: 1652
allele frequency: 1.937148217636022e-1
allele num: 8528
num of homozygotes: 166

African
type: Population
allele count: 306
allele frequency: 3.045988453115668e-2
allele num: 10046
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 8422
allele frequency: 1.306019911298577e-1
allele num: 64486
num of homozygotes: 528

South Asian
type: Population
allele count: 2262
allele frequency: 1.836933571544583e-1
allele num: 12314
num of homozygotes: 224

QD
type: SiteQuality
SIO_000300: 1.605e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

FS
type: SiteQuality
SIO_000300: 7.8e-1

DP
type: SiteQuality
SIO_000300: 1.687474e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.61e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
all individuals: 2343
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9347
bin: 9.75e1
variant carriers: 118

GenotypeQuality
all individuals: 352
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 668
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.522987493394399e-4
allele num: 11354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12170
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 24
allele frequency: 3.675344563552833e-3
allele num: 6530
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 1.210653753026634e-3
allele num: 826
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.970089730807577e-5
allele num: 10030
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 91
allele frequency: 1.409628849371089e-3
allele num: 64556
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.26e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

QD
type: SiteQuality
SIO_000300: 1.508e1

MQ
type: SiteQuality
SIO_000300: 5.979e1

DP
type: SiteQuality
SIO_000300: 1.710842e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

GenotypeQuality
all individuals: 447
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9347
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2601
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3157
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10030
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549042691616581e-5
allele num: 64556
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12170
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.26e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

DP
type: SiteQuality
SIO_000300: 1.710842e6

QD
type: SiteQuality
SIO_000300: 1.508e1

MQ
type: SiteQuality
SIO_000300: 5.979e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

GenotypeQuality
all individuals: 344
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 52368
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 268
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506477854775535e-5
allele num: 66380
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15664
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.662169e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.585e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.942e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: -8.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.24e-1

GenotypeQuality
all individuals: 720
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 52367
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1935
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506977304921788e-5
allele num: 66358
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15622
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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

DP
type: SiteQuality
SIO_000300: 6.664134e6

MQ
type: SiteQuality
SIO_000300: 5.884e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

QD
type: SiteQuality
SIO_000300: 1.774e1

FS
type: SiteQuality
SIO_000300: 1.001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.304e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.7e-2

GenotypeQuality
all individuals: 683
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
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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: 13
bin: 2.5e0
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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: 270
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variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 2.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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: 10394
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: 15760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66406
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 2.959e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.19e-1

QD
type: SiteQuality
SIO_000300: 1.054e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: 4.96e-1

DP
type: SiteQuality
SIO_000300: 6.667214e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

GenotypeQuality
all individuals: 449
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52367
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 2.5e0
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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

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: 1.504302304591131e-5
allele num: 66476
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-1

FS
type: SiteQuality
SIO_000300: 5.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

DP
type: SiteQuality
SIO_000300: 6.685591e6

QD
type: SiteQuality
SIO_000300: 1.27e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.74e-1

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

GenotypeQuality
all individuals: 557
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3585
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
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variant carriers: 0

GenotypeQuality
all individuals: 287
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
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variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52367
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504302304591131e-5
allele num: 66476
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: 1.27e1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

DP
type: SiteQuality
SIO_000300: 6.685591e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-1

FS
type: SiteQuality
SIO_000300: 5.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 437
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variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 221
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GenotypeQuality
all individuals: 1033
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 43
allele frequency: 3.715223777432176e-3
allele num: 11574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.209555488358028e-3
allele num: 6614
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.870324189526185e-4
allele num: 16040
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.057895749182535e-3
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 266
allele frequency: 4.000240615976901e-3
allele num: 66496
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

QD
type: SiteQuality
SIO_000300: 1.362e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

DP
type: SiteQuality
SIO_000300: 6.700813e6

VQSLOD
type: SiteQuality
SIO_000300: 4.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

GenotypeQuality
all individuals: 265
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 292
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 422
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GenotypeQuality
all individuals: 52362
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 191
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.006976184748617e-5
allele num: 66512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 16068
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.306e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.946e1

DP
type: SiteQuality
SIO_000300: 6.6982e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.35e-1

QD
type: SiteQuality
SIO_000300: 1.712e1

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52363
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3918
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GenotypeQuality
all individuals: 72
bin: 4.75e1
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GenotypeQuality
all individuals: 599
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GenotypeQuality
all individuals: 12
bin: 1.75e1
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GenotypeQuality
all individuals: 487
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GenotypeQuality
all individuals: 441
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GenotypeQuality
all individuals: 215
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
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variant carriers: 0

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

GenotypeQuality
all individuals: 1069
bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66530
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16094
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.5161e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.187e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.392e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: -7.695e0

QD
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 6.699053e6

MQ
type: SiteQuality
SIO_000300: 5.583e1

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.25e1
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GenotypeQuality
all individuals: 386
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 292
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3942
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16122
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.699757e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: -7.823e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.87e-1

FS
type: SiteQuality
SIO_000300: 8.4816e1

QD
type: SiteQuality
SIO_000300: 6.0e-2

MQ
type: SiteQuality
SIO_000300: 5.591e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.265e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.171e1

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

GenotypeQuality
all individuals: 212
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52363
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
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
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502810255177181e-5
allele num: 66542
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: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16150
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.17e-1

QD
type: SiteQuality
SIO_000300: 1.473e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 6.701047e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.399999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 644
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 52370
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.360000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.333e1

MQ
type: SiteQuality
SIO_000300: 5.93e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.07e0

FS
type: SiteQuality
SIO_000300: 4.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.23e-1

DP
type: SiteQuality
SIO_000300: 6.70778e6

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4351
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
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: 16344
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: 902
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.875e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

FS
type: SiteQuality
SIO_000300: 5.79e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.453e0

DP
type: SiteQuality
SIO_000300: 6.709184e6

GenotypeQuality
all individuals: 253
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
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variant carriers: 0

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

GenotypeQuality
all individuals: 52375
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 313
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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: 16406
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: -1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.462e0

QD
type: SiteQuality
SIO_000300: 1.847e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.197e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.711352e6