19-53612348-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612348
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612348
    reference: chr 19
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.260T>C
  hgvsp: ENSP00000472911.1:p.Leu87Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*826T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.911T>C
  hgvsp: ENSP00000414601.1:p.Leu304Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.950T>C
  hgvsp: ENSP00000243643.3:p.Leu317Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*826T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.986T>C
  hgvsp: ENSP00000395055.1:p.Leu329Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*826T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1094T>C
  hgvsp: ENSP00000388787.2:p.Leu365Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.950T>C
  hgvsp: ENSP00000439435.1:p.Leu317Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*991T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*826T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1094T>C
  hgvsp: ENSP00000396492.1:p.Leu365Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*991T>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7365
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu317Pro
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

19-53612359-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612359
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612359
    reference: chr 19
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*815A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*815A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*980A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1083A>G
  hgvsp: ENST00000455735.2:c.1083A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.939A>G
  hgvsp: ENST00000500065.4:c.939A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1083A>G
  hgvsp: ENST00000448501.1:c.1083A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.249A>G
  hgvsp: ENST00000601493.1:c.249A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.975A>G
  hgvsp: ENST00000421033.1:c.975A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*980A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.939A>G
  hgvsp: ENST00000243643.4:c.939A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.900A>G
  hgvsp: ENST00000440291.1:c.900A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*815A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*815A>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser313Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

19-53612366-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612366
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612366
    reference: chr 19
allele count: 5
allele frequency: 4.119837843182493e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*973G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.932G>A
  hgvsp: ENSP00000439435.1:p.Arg311Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1076G>A
  hgvsp: ENSP00000388787.2:p.Arg359Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.242G>A
  hgvsp: ENSP00000472911.1:p.Arg81Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1076G>A
  hgvsp: ENSP00000396492.1:p.Arg359Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*808G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.968G>A
  hgvsp: ENSP00000395055.1:p.Arg323Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*808G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.893G>A
  hgvsp: ENSP00000414601.1:p.Arg298Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*973G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.932G>A
  hgvsp: ENSP00000243643.3:p.Arg311Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*808G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*808G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg311Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

19-53612367-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612367
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612367
    reference: chr 19
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*807C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*972C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.892C>T
  hgvsp: ENSP00000414601.1:p.Arg298Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.931C>T
  hgvsp: ENSP00000439435.1:p.Arg311Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1075C>T
  hgvsp: ENSP00000396492.1:p.Arg359Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*807C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.967C>T
  hgvsp: ENSP00000395055.1:p.Arg323Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.241C>T
  hgvsp: ENSP00000472911.1:p.Arg81Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1075C>T
  hgvsp: ENSP00000388787.2:p.Arg359Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*807C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.931C>T
  hgvsp: ENSP00000243643.3:p.Arg311Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*972C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*807C>T
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg311Ter
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/19-53612372-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612372
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612372
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.236T>G
  hgvsp: ENSP00000472911.1:p.Phe79Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.926T>G
  hgvsp: ENSP00000439435.1:p.Phe309Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*802T>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1070T>G
  hgvsp: ENSP00000396492.1:p.Phe357Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.887T>G
  hgvsp: ENSP00000414601.1:p.Phe296Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*802T>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.926T>G
  hgvsp: ENSP00000243643.3:p.Phe309Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*967T>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.962T>G
  hgvsp: ENSP00000395055.1:p.Phe321Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1070T>G
  hgvsp: ENSP00000388787.2:p.Phe357Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*967T>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*802T>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*802T>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe309Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-53612376-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612376
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612376
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*798G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1066G>T
  hgvsp: ENSP00000396492.1:p.Val356Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.958G>T
  hgvsp: ENSP00000395055.1:p.Val320Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.883G>T
  hgvsp: ENSP00000414601.1:p.Val295Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*798G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*798G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1066G>T
  hgvsp: ENSP00000388787.2:p.Val356Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*798G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*963G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*963G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.922G>T
  hgvsp: ENSP00000439435.1:p.Val308Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.922G>T
  hgvsp: ENSP00000243643.3:p.Val308Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.232G>T
  hgvsp: ENSP00000472911.1:p.Val78Phe
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val308Phe
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

19-53612379-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612379
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612379
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.919A>G
  hgvsp: ENSP00000439435.1:p.Lys307Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.880A>G
  hgvsp: ENSP00000414601.1:p.Lys294Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*795A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*795A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.955A>G
  hgvsp: ENSP00000395055.1:p.Lys319Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*960A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1063A>G
  hgvsp: ENSP00000396492.1:p.Lys355Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1063A>G
  hgvsp: ENSP00000388787.2:p.Lys355Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.229A>G
  hgvsp: ENSP00000472911.1:p.Lys77Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*960A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*795A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*795A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.919A>G
  hgvsp: ENSP00000243643.3:p.Lys307Glu
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys307Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

19-53612380-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612380
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612380
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.228C>G
  hgvsp: ENSP00000472911.1:p.Asp76Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.954C>G
  hgvsp: ENSP00000395055.1:p.Asp318Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1062C>G
  hgvsp: ENSP00000396492.1:p.Asp354Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.918C>G
  hgvsp: ENSP00000243643.3:p.Asp306Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1062C>G
  hgvsp: ENSP00000388787.2:p.Asp354Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*794C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*794C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.879C>G
  hgvsp: ENSP00000414601.1:p.Asp293Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*794C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*959C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.918C>G
  hgvsp: ENSP00000439435.1:p.Asp306Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*794C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*959C>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp306Glu
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

19-53612380-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612380
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612380
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.228C>A
  hgvsp: ENSP00000472911.1:p.Asp76Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*794C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*959C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*794C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1062C>A
  hgvsp: ENSP00000388787.2:p.Asp354Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*794C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.879C>A
  hgvsp: ENSP00000414601.1:p.Asp293Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.954C>A
  hgvsp: ENSP00000395055.1:p.Asp318Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1062C>A
  hgvsp: ENSP00000396492.1:p.Asp354Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*794C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.918C>A
  hgvsp: ENSP00000243643.3:p.Asp306Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.918C>A
  hgvsp: ENSP00000439435.1:p.Asp306Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*959C>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp306Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

19-53612382-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612382
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612382
    reference: chr 19
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.952G>C
  hgvsp: ENSP00000395055.1:p.Asp318His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1060G>C
  hgvsp: ENSP00000396492.1:p.Asp354His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.877G>C
  hgvsp: ENSP00000414601.1:p.Asp293His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.916G>C
  hgvsp: ENSP00000243643.3:p.Asp306His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*792G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*792G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1060G>C
  hgvsp: ENSP00000388787.2:p.Asp354His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*792G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*957G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*957G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.916G>C
  hgvsp: ENSP00000439435.1:p.Asp306His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.226G>C
  hgvsp: ENSP00000472911.1:p.Asp76His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*792G>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5466
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp306His
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

19-53612414-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612414
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612414
    reference: chr 19
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.920C>T
  hgvsp: ENSP00000395055.1:p.Thr307Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1028C>T
  hgvsp: ENSP00000396492.1:p.Thr343Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.194C>T
  hgvsp: ENSP00000472911.1:p.Thr65Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1028C>T
  hgvsp: ENSP00000388787.2:p.Thr343Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*760C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.884C>T
  hgvsp: ENSP00000243643.3:p.Thr295Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.845C>T
  hgvsp: ENSP00000414601.1:p.Thr282Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*760C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*925C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.884C>T
  hgvsp: ENSP00000439435.1:p.Thr295Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*760C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*925C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*760C>T
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr295Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

19-53612421-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612421
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612421
    reference: chr 19
allele count: 3
allele frequency: 2.471495419495156e-5
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.913G>A
  hgvsp: ENSP00000395055.1:p.Val305Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.877G>A
  hgvsp: ENSP00000243643.3:p.Val293Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.877G>A
  hgvsp: ENSP00000439435.1:p.Val293Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*918G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1021G>A
  hgvsp: ENSP00000396492.1:p.Val341Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*753G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*753G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.838G>A
  hgvsp: ENSP00000414601.1:p.Val280Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*753G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*753G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*918G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1021G>A
  hgvsp: ENSP00000388787.2:p.Val341Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.187G>A
  hgvsp: ENSP00000472911.1:p.Val63Ile
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7393
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val293Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP

19-53612423-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612423
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612423
    reference: chr 19
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*751G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.911G>C
  hgvsp: ENSP00000395055.1:p.Arg304Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.875G>C
  hgvsp: ENSP00000439435.1:p.Arg292Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*916G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.875G>C
  hgvsp: ENSP00000243643.3:p.Arg292Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*751G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*751G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1019G>C
  hgvsp: ENSP00000396492.1:p.Arg340Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.185G>C
  hgvsp: ENSP00000472911.1:p.Arg62Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.836G>C
  hgvsp: ENSP00000414601.1:p.Arg279Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1019G>C
  hgvsp: ENSP00000388787.2:p.Arg340Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*916G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*751G>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg292Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum

19-53612426-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612426
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612426
    reference: chr 19
allele count: 11
allele frequency: 9.062299187688454e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*913G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*748G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*913G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*748G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.182G>A
  hgvsp: ENSP00000472911.1:p.Arg61Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.833G>A
  hgvsp: ENSP00000414601.1:p.Arg278Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*748G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.872G>A
  hgvsp: ENSP00000439435.1:p.Arg291Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1016G>A
  hgvsp: ENSP00000388787.2:p.Arg339Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*748G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.872G>A
  hgvsp: ENSP00000243643.3:p.Arg291Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1016G>A
  hgvsp: ENSP00000396492.1:p.Arg339Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.908G>A
  hgvsp: ENSP00000395055.1:p.Arg303Gln
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3319
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg291Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ

19-53612427-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612427
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612427
    reference: chr 19
allele count: 5
allele frequency: 4.119159032491926e-5
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1015C>T
  hgvsp: ENSP00000388787.2:p.Arg339Trp
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*912C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.832C>T
  hgvsp: ENSP00000414601.1:p.Arg278Trp
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.181C>T
  hgvsp: ENSP00000472911.1:p.Arg61Trp
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1015C>T
  hgvsp: ENSP00000396492.1:p.Arg339Trp
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*747C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*912C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.907C>T
  hgvsp: ENSP00000395055.1:p.Arg303Trp
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*747C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.871C>T
  hgvsp: ENSP00000439435.1:p.Arg291Trp
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.871C>T
  hgvsp: ENSP00000243643.3:p.Arg291Trp
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*747C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*747C>T
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg291Trp
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

19-53612431-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612431
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612431
    reference: chr 19
allele count: 18
allele frequency: 1.482848386990477e-4
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.828A>G
  hgvsp: ENST00000440291.1:c.828A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1011A>G
  hgvsp: ENST00000455735.2:c.1011A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.903A>G
  hgvsp: ENST00000421033.1:c.903A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.867A>G
  hgvsp: ENST00000243643.4:c.867A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.177A>G
  hgvsp: ENST00000601493.1:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*743A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*743A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1011A>G
  hgvsp: ENST00000448501.1:c.1011A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*743A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*908A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*743A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*908A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.867A>G
  hgvsp: ENST00000500065.4:c.867A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu289Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

19-53612432-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612432
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612432
    reference: chr 19
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.902T>C
  hgvsp: ENSP00000395055.1:p.Leu301Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1010T>C
  hgvsp: ENSP00000388787.2:p.Leu337Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*742T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*742T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.827T>C
  hgvsp: ENSP00000414601.1:p.Leu276Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.866T>C
  hgvsp: ENSP00000243643.3:p.Leu289Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*742T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1010T>C
  hgvsp: ENSP00000396492.1:p.Leu337Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.176T>C
  hgvsp: ENSP00000472911.1:p.Leu59Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*907T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*742T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.866T>C
  hgvsp: ENSP00000439435.1:p.Leu289Pro
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*907T>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu289Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

19-53612436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612436
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612436
    reference: chr 19
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*903G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1006G>A
  hgvsp: ENSP00000388787.2:p.Ala336Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.898G>A
  hgvsp: ENSP00000395055.1:p.Ala300Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*738G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.862G>A
  hgvsp: ENSP00000243643.3:p.Ala288Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1006G>A
  hgvsp: ENSP00000396492.1:p.Ala336Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*738G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.823G>A
  hgvsp: ENSP00000414601.1:p.Ala275Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.862G>A
  hgvsp: ENSP00000439435.1:p.Ala288Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*738G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.172G>A
  hgvsp: ENSP00000472911.1:p.Ala58Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*903G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*738G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala288Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

19-53612437-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612437
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612437
    reference: chr 19
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.861T>C
  hgvsp: ENST00000243643.4:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*902T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*737T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*737T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.861T>C
  hgvsp: ENST00000500065.4:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.171T>C
  hgvsp: ENST00000601493.1:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*902T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1005T>C
  hgvsp: ENST00000455735.2:c.1005T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.897T>C
  hgvsp: ENST00000421033.1:c.897T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.822T>C
  hgvsp: ENST00000440291.1:c.822T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*737T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1005T>C
  hgvsp: ENST00000448501.1:c.1005T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*737T>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu287Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

19-53612441-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612441
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612441
    reference: chr 19
allele count: 3
allele frequency: 2.471536142096851e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.1001G>A
  hgvsp: ENSP00000388787.2:p.Cys334Tyr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.857G>A
  hgvsp: ENSP00000439435.1:p.Cys286Tyr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*733G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.857G>A
  hgvsp: ENSP00000243643.3:p.Cys286Tyr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*733G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.167G>A
  hgvsp: ENSP00000472911.1:p.Cys56Tyr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.893G>A
  hgvsp: ENSP00000395055.1:p.Cys298Tyr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.818G>A
  hgvsp: ENSP00000414601.1:p.Cys273Tyr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.1001G>A
  hgvsp: ENSP00000396492.1:p.Cys334Tyr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*733G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*898G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*898G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*733G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys286Tyr
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

19-53612443-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612443
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612443
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.999A>G
  hgvsp: ENST00000455735.2:c.999A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*731A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*731A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*896A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.816A>G
  hgvsp: ENST00000440291.1:c.816A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.855A>G
  hgvsp: ENST00000500065.4:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.999A>G
  hgvsp: ENST00000448501.1:c.999A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*731A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.891A>G
  hgvsp: ENST00000421033.1:c.891A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.165A>G
  hgvsp: ENST00000601493.1:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*731A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.855A>G
  hgvsp: ENST00000243643.4:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*896A>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser285Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

19-53612445-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612445
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612445
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*729T>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.853T>A
  hgvsp: ENSP00000243643.3:p.Ser285Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.853T>A
  hgvsp: ENSP00000439435.1:p.Ser285Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.889T>A
  hgvsp: ENSP00000395055.1:p.Ser297Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*729T>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.814T>A
  hgvsp: ENSP00000414601.1:p.Ser272Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*894T>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.997T>A
  hgvsp: ENSP00000388787.2:p.Ser333Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*729T>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.163T>A
  hgvsp: ENSP00000472911.1:p.Ser55Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*894T>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.997T>A
  hgvsp: ENSP00000396492.1:p.Ser333Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*729T>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser285Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

19-53612450-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612450
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612450
    reference: chr 19
allele count: 5
allele frequency: 4.11936265221045e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*724G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.992G>A
  hgvsp: ENSP00000396492.1:p.Arg331His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.848G>A
  hgvsp: ENSP00000243643.3:p.Arg283His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*724G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.992G>A
  hgvsp: ENSP00000388787.2:p.Arg331His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.158G>A
  hgvsp: ENSP00000472911.1:p.Arg53His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*889G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.848G>A
  hgvsp: ENSP00000439435.1:p.Arg283His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.809G>A
  hgvsp: ENSP00000414601.1:p.Arg270His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.884G>A
  hgvsp: ENSP00000395055.1:p.Arg295His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*724G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*724G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*889G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg283His
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

19-53612451-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612451
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612451
    reference: chr 19
allele count: 20
allele frequency: 1.647663612996771e-4
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.847C>T
  hgvsp: ENSP00000243643.3:p.Arg283Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.847C>T
  hgvsp: ENSP00000439435.1:p.Arg283Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.991C>T
  hgvsp: ENSP00000388787.2:p.Arg331Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*723C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*723C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*888C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.883C>T
  hgvsp: ENSP00000395055.1:p.Arg295Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.808C>T
  hgvsp: ENSP00000414601.1:p.Arg270Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.991C>T
  hgvsp: ENSP00000396492.1:p.Arg331Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*723C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.157C>T
  hgvsp: ENSP00000472911.1:p.Arg53Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*723C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*888C>T
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg283Cys
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS

19-53612469-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612469
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612469
    reference: chr 19
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.973T>C
  hgvsp: ENSP00000396492.1:p.Cys325Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*870T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*705T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.829T>C
  hgvsp: ENSP00000439435.1:p.Cys277Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.973T>C
  hgvsp: ENSP00000388787.2:p.Cys325Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.790T>C
  hgvsp: ENSP00000414601.1:p.Cys264Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*870T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.865T>C
  hgvsp: ENSP00000395055.1:p.Cys289Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.139T>C
  hgvsp: ENSP00000472911.1:p.Cys47Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*705T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*705T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*705T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.829T>C
  hgvsp: ENSP00000243643.3:p.Cys277Arg
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys277Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

19-53612472-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612472
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612472
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.970G>C
  hgvsp: ENSP00000396492.1:p.Glu324Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*867G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.787G>C
  hgvsp: ENSP00000414601.1:p.Glu263Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.862G>C
  hgvsp: ENSP00000395055.1:p.Glu288Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.970G>C
  hgvsp: ENSP00000388787.2:p.Glu324Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*702G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.136G>C
  hgvsp: ENSP00000472911.1:p.Glu46Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.826G>C
  hgvsp: ENSP00000439435.1:p.Glu276Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.826G>C
  hgvsp: ENSP00000243643.3:p.Glu276Gln
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*867G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*702G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*702G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*702G>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu276Gln
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

19-53612473-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612473
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612473
    reference: chr 19
allele count: 8
allele frequency: 6.590654451987082e-5
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*701T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*701T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.825T>C
  hgvsp: ENST00000243643.4:c.825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.861T>C
  hgvsp: ENST00000421033.1:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*866T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.969T>C
  hgvsp: ENST00000448501.1:c.969T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.969T>C
  hgvsp: ENST00000455735.2:c.969T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*866T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.135T>C
  hgvsp: ENST00000601493.1:c.135T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*701T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.786T>C
  hgvsp: ENST00000440291.1:c.786T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*701T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.825T>C
  hgvsp: ENST00000500065.4:c.825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn275Asn
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum

19-53612485-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612485
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612485
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.849A>G
  hgvsp: ENST00000421033.1:c.849A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.813A>G
  hgvsp: ENST00000500065.4:c.813A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.774A>G
  hgvsp: ENST00000440291.1:c.774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.957A>G
  hgvsp: ENST00000448501.1:c.957A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*689A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.813A>G
  hgvsp: ENST00000243643.4:c.813A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.957A>G
  hgvsp: ENST00000455735.2:c.957A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*689A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.123A>G
  hgvsp: ENST00000601493.1:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*689A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*689A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*854A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*854A>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro271Pro
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

19-53612490-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612490
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612490
    reference: chr 19
allele count: 463
allele frequency: 3.81390138223035e-3
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.844A>G
  hgvsp: ENSP00000395055.1:p.Lys282Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*849A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.808A>G
  hgvsp: ENSP00000243643.3:p.Lys270Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.808A>G
  hgvsp: ENSP00000439435.1:p.Lys270Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*684A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.952A>G
  hgvsp: ENSP00000388787.2:p.Lys318Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.769A>G
  hgvsp: ENSP00000414601.1:p.Lys257Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*684A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*684A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.118A>G
  hgvsp: ENSP00000472911.1:p.Lys40Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.952A>G
  hgvsp: ENSP00000396492.1:p.Lys318Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*849A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*684A>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 6.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 5.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 9.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 7.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 4.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys270Glu
num of homozygotes: 2
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-53612496-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612496
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612496
    reference: chr 19
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*678G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.112G>A
  hgvsp: ENSP00000472911.1:p.Gly38Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.946G>A
  hgvsp: ENSP00000396492.1:p.Gly316Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.802G>A
  hgvsp: ENSP00000439435.1:p.Gly268Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.763G>A
  hgvsp: ENSP00000414601.1:p.Gly255Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*678G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*678G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*678G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.802G>A
  hgvsp: ENSP00000243643.3:p.Gly268Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.946G>A
  hgvsp: ENSP00000388787.2:p.Gly316Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.838G>A
  hgvsp: ENSP00000395055.1:p.Gly280Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*843G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*843G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5579
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly268Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

19-53612497-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612497
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612497
    reference: chr 19
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*677T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*842T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*677T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.762T>C
  hgvsp: ENST00000440291.1:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*842T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.945T>C
  hgvsp: ENST00000455735.2:c.945T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.111T>C
  hgvsp: ENST00000601493.1:c.111T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.945T>C
  hgvsp: ENST00000448501.1:c.945T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.801T>C
  hgvsp: ENST00000500065.4:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.801T>C
  hgvsp: ENST00000243643.4:c.801T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*677T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.837T>C
  hgvsp: ENST00000421033.1:c.837T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*677T>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7429
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr267Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-53612505-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612505
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612505
    reference: chr 19
allele count: 3
allele frequency: 2.47133254250692e-5
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.793G>C
  hgvsp: ENSP00000243643.3:p.Val265Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*669G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*669G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.937G>C
  hgvsp: ENSP00000396492.1:p.Val313Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.754G>C
  hgvsp: ENSP00000414601.1:p.Val252Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*834G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*669G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.103G>C
  hgvsp: ENSP00000472911.1:p.Val35Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.937G>C
  hgvsp: ENSP00000388787.2:p.Val313Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*834G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.829G>C
  hgvsp: ENSP00000395055.1:p.Val277Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.793G>C
  hgvsp: ENSP00000439435.1:p.Val265Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*669G>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val265Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-53612516-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612516
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612516
    reference: chr 19
allele count: 11
allele frequency: 9.06140336425194e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*823G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*658G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.782G>A
  hgvsp: ENSP00000243643.3:p.Arg261His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*658G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.926G>A
  hgvsp: ENSP00000396492.1:p.Arg309His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.743G>A
  hgvsp: ENSP00000414601.1:p.Arg248His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.818G>A
  hgvsp: ENSP00000395055.1:p.Arg273His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*658G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.782G>A
  hgvsp: ENSP00000439435.1:p.Arg261His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.926G>A
  hgvsp: ENSP00000388787.2:p.Arg309His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.92G>A
  hgvsp: ENSP00000472911.1:p.Arg31His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*823G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*658G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg261His
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/19-53612518-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612518
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612518
    reference: chr 19
allele count: 12
allele frequency: 9.885004448252002e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.924G>T
  hgvsp: ENST00000455735.2:c.924G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*656G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.816G>T
  hgvsp: ENST00000421033.1:c.816G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*821G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.780G>T
  hgvsp: ENST00000500065.4:c.780G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*656G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.780G>T
  hgvsp: ENST00000243643.4:c.780G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.741G>T
  hgvsp: ENST00000440291.1:c.741G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.924G>T
  hgvsp: ENST00000448501.1:c.924G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*821G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*656G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.90G>T
  hgvsp: ENST00000601493.1:c.90G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*656G>T
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala260Ala
num of homozygotes: 1
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

19-53612518-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612518
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612518
    reference: chr 19
allele count: 180
allele frequency: 1.4827506672378e-3
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.924G>A
  hgvsp: ENST00000448501.1:c.924G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*821G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.90G>A
  hgvsp: ENST00000601493.1:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*656G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*656G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.780G>A
  hgvsp: ENST00000500065.4:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*821G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*656G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.924G>A
  hgvsp: ENST00000455735.2:c.924G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.741G>A
  hgvsp: ENST00000440291.1:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*656G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.816G>A
  hgvsp: ENST00000421033.1:c.816G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.780G>A
  hgvsp: ENST00000243643.4:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 6.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 8.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: p.Ala260Ala
num of homozygotes: 2
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ

19-53612519-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612519
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612519
    reference: chr 19
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*655C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*655C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.89C>T
  hgvsp: ENSP00000472911.1:p.Ala30Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.923C>T
  hgvsp: ENSP00000388787.2:p.Ala308Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.740C>T
  hgvsp: ENSP00000414601.1:p.Ala247Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*820C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.779C>T
  hgvsp: ENSP00000439435.1:p.Ala260Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.923C>T
  hgvsp: ENSP00000396492.1:p.Ala308Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*820C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.815C>T
  hgvsp: ENSP00000395055.1:p.Ala272Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.779C>T
  hgvsp: ENSP00000243643.3:p.Ala260Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*655C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*655C>T
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala260Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

http://identifiers.org/exac.variant/19-53612520-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612520
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612519
    reference: chr 19
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.921delT
  hgvsp: ENSP00000388787.2:p.Ala308ArgfsTer80
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*653delT
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.87delT
  hgvsp: ENSP00000472911.1:p.Ala30ArgfsTer80
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*653delT
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*818delT
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*653delT
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.738delT
  hgvsp: ENSP00000414601.1:p.Ala247ArgfsTer80
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.813delT
  hgvsp: ENSP00000395055.1:p.Ala272ArgfsTer80
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*653delT
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.921delT
  hgvsp: ENSP00000396492.1:p.Ala308ArgfsTer80
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.777delT
  hgvsp: ENSP00000439435.1:p.Ala260ArgfsTer80
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*818delT
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.777delT
  hgvsp: ENSP00000243643.3:p.Ala260ArgfsTer80
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4248
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala260ArgfsTer80
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CA
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

19-53612524-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612524
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612524
    reference: chr 19
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.774C>A
  hgvsp: ENSP00000243643.3:p.Asn258Lys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.735C>A
  hgvsp: ENSP00000414601.1:p.Asn245Lys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.918C>A
  hgvsp: ENSP00000396492.1:p.Asn306Lys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.84C>A
  hgvsp: ENSP00000472911.1:p.Asn28Lys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.774C>A
  hgvsp: ENSP00000439435.1:p.Asn258Lys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*815C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*650C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.810C>A
  hgvsp: ENSP00000395055.1:p.Asn270Lys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.918C>A
  hgvsp: ENSP00000388787.2:p.Asn306Lys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*650C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*650C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*650C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*815C>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn258Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

19-53612544-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612544
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612544
    reference: chr 19
allele count: 12
allele frequency: 9.884353069091628e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*630G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.898G>A
  hgvsp: ENSP00000388787.2:p.Val300Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.754G>A
  hgvsp: ENSP00000439435.1:p.Val252Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.898G>A
  hgvsp: ENSP00000396492.1:p.Val300Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*630G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*630G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.790G>A
  hgvsp: ENSP00000395055.1:p.Val264Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.754G>A
  hgvsp: ENSP00000243643.3:p.Val252Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.715G>A
  hgvsp: ENSP00000414601.1:p.Val239Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.64G>A
  hgvsp: ENSP00000472911.1:p.Val22Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*795G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*630G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*795G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4248
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Val252Ile
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum

19-53612548-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612548
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612548
    reference: chr 19
allele count: 9
allele frequency: 7.421945869274793e-5
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.750C>A
  hgvsp: ENST00000500065.4:c.750C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.894C>A
  hgvsp: ENST00000448501.1:c.894C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.786C>A
  hgvsp: ENST00000421033.1:c.786C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*626C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*626C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.60C>A
  hgvsp: ENST00000601493.1:c.60C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.711C>A
  hgvsp: ENST00000440291.1:c.711C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.894C>A
  hgvsp: ENST00000455735.2:c.894C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*791C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.750C>A
  hgvsp: ENST00000243643.4:c.750C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*626C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*626C>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*791C>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly250Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

19-53612554-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612554
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612554
    reference: chr 19
allele count: 5
allele frequency: 4.118616144975288e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.888G>A
  hgvsp: ENST00000448501.1:c.888G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.888G>A
  hgvsp: ENST00000455735.2:c.888G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.744G>A
  hgvsp: ENST00000500065.4:c.744G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.780G>A
  hgvsp: ENST00000421033.1:c.780G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.744G>A
  hgvsp: ENST00000243643.4:c.744G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.54G>A
  hgvsp: ENST00000601493.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*620G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.705G>A
  hgvsp: ENST00000440291.1:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*620G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*785G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*785G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*620G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*620G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu248Leu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

19-53612558-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612558
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612558
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.50A>G
  hgvsp: ENSP00000472911.1:p.Asp17Gly
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*616A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.701A>G
  hgvsp: ENSP00000414601.1:p.Asp234Gly
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.740A>G
  hgvsp: ENSP00000243643.3:p.Asp247Gly
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.884A>G
  hgvsp: ENSP00000396492.1:p.Asp295Gly
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.884A>G
  hgvsp: ENSP00000388787.2:p.Asp295Gly
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.740A>G
  hgvsp: ENSP00000439435.1:p.Asp247Gly
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*781A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.776A>G
  hgvsp: ENSP00000395055.1:p.Asp259Gly
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*616A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*616A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*781A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*616A>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp247Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-53612561-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612561
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612561
    reference: chr 19
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*613G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.698G>T
  hgvsp: ENSP00000414601.1:p.Cys233Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.773G>T
  hgvsp: ENSP00000395055.1:p.Cys258Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*613G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.737G>T
  hgvsp: ENSP00000439435.1:p.Cys246Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*613G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.881G>T
  hgvsp: ENSP00000388787.2:p.Cys294Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*778G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.737G>T
  hgvsp: ENSP00000243643.3:p.Cys246Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.47G>T
  hgvsp: ENSP00000472911.1:p.Cys16Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*613G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.881G>T
  hgvsp: ENSP00000396492.1:p.Cys294Phe
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*778G>T
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys246Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD

19-53612562-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612562
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612562
    reference: chr 19
allele count: 23
allele frequency: 1.894532215284756e-4
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.880T>C
  hgvsp: ENSP00000396492.1:p.Cys294Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.772T>C
  hgvsp: ENSP00000395055.1:p.Cys258Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*612T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.46T>C
  hgvsp: ENSP00000472911.1:p.Cys16Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*612T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.697T>C
  hgvsp: ENSP00000414601.1:p.Cys233Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*612T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.736T>C
  hgvsp: ENSP00000243643.3:p.Cys246Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*777T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.880T>C
  hgvsp: ENSP00000388787.2:p.Cys294Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.736T>C
  hgvsp: ENSP00000439435.1:p.Cys246Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*612T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*777T>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys246Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

19-53612565-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612565
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612565
    reference: chr 19
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.733A>G
  hgvsp: ENSP00000243643.3:p.Lys245Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*609A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*609A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*774A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.877A>G
  hgvsp: ENSP00000396492.1:p.Lys293Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.694A>G
  hgvsp: ENSP00000414601.1:p.Lys232Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*774A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.43A>G
  hgvsp: ENSP00000472911.1:p.Lys15Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.769A>G
  hgvsp: ENSP00000395055.1:p.Lys257Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*609A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.733A>G
  hgvsp: ENSP00000439435.1:p.Lys245Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.877A>G
  hgvsp: ENSP00000388787.2:p.Lys293Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*609A>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys245Glu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP

19-53612569-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612569
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612569
    reference: chr 19
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.690A>T
  hgvsp: ENST00000440291.1:c.690A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*605A>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.873A>T
  hgvsp: ENST00000455735.2:c.873A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*605A>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*770A>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.729A>T
  hgvsp: ENST00000500065.4:c.729A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.39A>T
  hgvsp: ENST00000601493.1:c.39A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.873A>T
  hgvsp: ENST00000448501.1:c.873A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*605A>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*770A>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.729A>T
  hgvsp: ENST00000243643.4:c.729A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.765A>T
  hgvsp: ENST00000421033.1:c.765A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*605A>T
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly243Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

19-53612571-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612571
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612569
    reference: chr 19
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.35_36delAA
  hgvsp: ENSP00000472911.1:p.Lys12ArgfsTer3
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*601_*602delAA
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.725_726delAA
  hgvsp: ENSP00000243643.3:p.Lys242ArgfsTer3
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.761_762delAA
  hgvsp: ENSP00000395055.1:p.Lys254ArgfsTer3
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*601_*602delAA
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*766_*767delAA
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.725_726delAA
  hgvsp: ENSP00000439435.1:p.Lys242ArgfsTer3
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.869_870delAA
  hgvsp: ENSP00000388787.2:p.Lys290ArgfsTer3
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.686_687delAA
  hgvsp: ENSP00000414601.1:p.Lys229ArgfsTer3
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.869_870delAA
  hgvsp: ENSP00000396492.1:p.Lys290ArgfsTer3
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*766_*767delAA
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*601_*602delAA
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*601_*602delAA
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys242ArgfsTer3
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: CTT
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

19-53612585-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612585
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612585
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*754A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*754A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.713A>G
  hgvsp: ENSP00000439435.1:p.His238Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.23A>G
  hgvsp: ENSP00000472911.1:p.His8Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.857A>G
  hgvsp: ENSP00000396492.1:p.His286Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.749A>G
  hgvsp: ENSP00000395055.1:p.His250Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.713A>G
  hgvsp: ENSP00000243643.3:p.His238Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*589A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.674A>G
  hgvsp: ENSP00000414601.1:p.His225Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.857A>G
  hgvsp: ENSP00000388787.2:p.His286Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*589A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*589A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*589A>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His238Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

19-53612590-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612590
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612590
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.669A>T
  hgvsp: ENST00000440291.1:c.669A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.708A>T
  hgvsp: ENST00000243643.4:c.708A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.744A>T
  hgvsp: ENST00000421033.1:c.744A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.708A>T
  hgvsp: ENST00000500065.4:c.708A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.852A>T
  hgvsp: ENST00000455735.2:c.852A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*584A>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*584A>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*749A>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.852A>T
  hgvsp: ENST00000448501.1:c.852A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*584A>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.18A>T
  hgvsp: ENST00000601493.1:c.18A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*749A>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*584A>T
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val236Val
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/19-53612592-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612592
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612592
    reference: chr 19
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*747G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.850G>T
  hgvsp: ENSP00000388787.2:p.Val284Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.850G>T
  hgvsp: ENSP00000396492.1:p.Val284Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*582G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*747G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*582G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.706G>T
  hgvsp: ENSP00000243643.3:p.Val236Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.742G>T
  hgvsp: ENSP00000395055.1:p.Val248Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.667G>T
  hgvsp: ENSP00000414601.1:p.Val223Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.706G>T
  hgvsp: ENSP00000439435.1:p.Val236Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*582G>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.16G>T
  hgvsp: ENSP00000472911.1:p.Val6Leu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*582G>T
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val236Leu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

19-53612593-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612593
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612593
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.741G>A
  hgvsp: ENST00000421033.1:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.849G>A
  hgvsp: ENST00000448501.1:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.849G>A
  hgvsp: ENST00000455735.2:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*581G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.15G>A
  hgvsp: ENST00000601493.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*581G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*581G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*746G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.705G>A
  hgvsp: ENST00000500065.4:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.666G>A
  hgvsp: ENST00000440291.1:c.666G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.705G>A
  hgvsp: ENST00000243643.4:c.705G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*581G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*746G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4625
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln235Gln
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-53612597-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612597
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612597
    reference: chr 19
allele count: 29
allele frequency: 2.388758010576432e-4
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.701G>A
  hgvsp: ENSP00000439435.1:p.Arg234His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.662G>A
  hgvsp: ENSP00000414601.1:p.Arg221His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*742G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.845G>A
  hgvsp: ENSP00000396492.1:p.Arg282His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*577G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*577G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.845G>A
  hgvsp: ENSP00000388787.2:p.Arg282His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.11G>A
  hgvsp: ENSP00000472911.1:p.Arg4His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.701G>A
  hgvsp: ENSP00000243643.3:p.Arg234His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*742G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*577G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.737G>A
  hgvsp: ENSP00000395055.1:p.Arg246His
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*577G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg234His
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

19-53612598-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612598
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612598
    reference: chr 19
allele count: 10
allele frequency: 8.237096588194593e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.844C>T
  hgvsp: ENSP00000388787.2:p.Arg282Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.700C>T
  hgvsp: ENSP00000243643.3:p.Arg234Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*741C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*576C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.700C>T
  hgvsp: ENSP00000439435.1:p.Arg234Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.10C>T
  hgvsp: ENSP00000472911.1:p.Arg4Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.661C>T
  hgvsp: ENSP00000414601.1:p.Arg221Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*576C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.844C>T
  hgvsp: ENSP00000396492.1:p.Arg282Cys
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*576C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*576C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*741C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.736C>T
  hgvsp: ENSP00000395055.1:p.Arg246Cys
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg234Cys
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

19-53612599-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612599
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612599
    reference: chr 19
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*575A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.843A>G
  hgvsp: ENST00000448501.1:c.843A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.699A>G
  hgvsp: ENST00000243643.4:c.699A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*575A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*740A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.660A>G
  hgvsp: ENST00000440291.1:c.660A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*575A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.699A>G
  hgvsp: ENST00000500065.4:c.699A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.843A>G
  hgvsp: ENST00000455735.2:c.843A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.9A>G
  hgvsp: ENST00000601493.1:c.9A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*575A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.735A>G
  hgvsp: ENST00000421033.1:c.735A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*740A>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val233Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

19-53612599-TAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612599
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612597
    reference: chr 19
allele count: 12
allele frequency: 9.884515905833511e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.697_698delGT
  hgvsp: ENSP00000243643.3:p.Val233ThrfsTer12
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.7_8delGT
  hgvsp: ENSP00000472911.1:p.Val3ThrfsTer12
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*573_*574delGT
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.733_734delGT
  hgvsp: ENSP00000395055.1:p.Val245ThrfsTer12
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*573_*574delGT
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.697_698delGT
  hgvsp: ENSP00000439435.1:p.Val233ThrfsTer12
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*738_*739delGT
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.658_659delGT
  hgvsp: ENSP00000414601.1:p.Val220ThrfsTer12
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.841_842delGT
  hgvsp: ENSP00000396492.1:p.Val281ThrfsTer12
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.841_842delGT
  hgvsp: ENSP00000388787.2:p.Val281ThrfsTer12
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*573_*574delGT
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*573_*574delGT
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*738_*739delGT
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val233ThrfsTer12
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: TAC
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP

19-53612601-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612601
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612601
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.733G>A
  hgvsp: ENSP00000395055.1:p.Val245Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.697G>A
  hgvsp: ENSP00000439435.1:p.Val233Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*738G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.841G>A
  hgvsp: ENSP00000396492.1:p.Val281Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.697G>A
  hgvsp: ENSP00000243643.3:p.Val233Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.658G>A
  hgvsp: ENSP00000414601.1:p.Val220Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.841G>A
  hgvsp: ENSP00000388787.2:p.Val281Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*573G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.7G>A
  hgvsp: ENSP00000472911.1:p.Val3Ile
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*738G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*573G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*573G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*573G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val233Ile
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

19-53612609-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612609
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612609
    reference: chr 19
allele count: 50
allele frequency: 4.118616144975288e-4
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.689A>G
  hgvsp: ENSP00000243643.3:p.His230Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.725A>G
  hgvsp: ENSP00000395055.1:p.His242Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*730A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.833A>G
  hgvsp: ENSP00000396492.1:p.His278Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*565A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.833A>G
  hgvsp: ENSP00000388787.2:p.His278Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.650A>G
  hgvsp: ENSP00000414601.1:p.His217Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.-2A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.689A>G
  hgvsp: ENSP00000439435.1:p.His230Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*565A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*565A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*730A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*565A>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 9.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 7407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His230Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

19-53612632-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612632
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612632
    reference: chr 19
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.810C>G
  hgvsp: ENSP00000396492.1:p.Asp270Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.810C>G
  hgvsp: ENSP00000388787.2:p.Asp270Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*542C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*542C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.666C>G
  hgvsp: ENSP00000439435.1:p.Asp222Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.-25C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*707C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.627C>G
  hgvsp: ENSP00000414601.1:p.Asp209Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*707C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.666C>G
  hgvsp: ENSP00000243643.3:p.Asp222Glu
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*542C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*542C>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.702C>G
  hgvsp: ENSP00000395055.1:p.Asp234Glu
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp222Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP

19-53612634-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612634
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612634
    reference: chr 19
allele count: 6
allele frequency: 4.94274651948266e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*540G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*540G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.625G>A
  hgvsp: ENSP00000414601.1:p.Asp209Asn
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.808G>A
  hgvsp: ENSP00000388787.2:p.Asp270Asn
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.664G>A
  hgvsp: ENSP00000439435.1:p.Asp222Asn
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.-27G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.664G>A
  hgvsp: ENSP00000243643.3:p.Asp222Asn
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.808G>A
  hgvsp: ENSP00000396492.1:p.Asp270Asn
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.700G>A
  hgvsp: ENSP00000395055.1:p.Asp234Asn
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*705G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*705G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*540G>A
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*540G>A
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5135
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp222Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

19-53612635-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612635
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612635
    reference: chr 19
allele count: 6
allele frequency: 4.942909396470763e-5
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*539C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.699C>T
  hgvsp: ENST00000421033.1:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.624C>T
  hgvsp: ENST00000440291.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.663C>T
  hgvsp: ENST00000243643.4:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*539C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*539C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.807C>T
  hgvsp: ENST00000448501.1:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.807C>T
  hgvsp: ENST00000455735.2:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*704C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.-28C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*539C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*704C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.663C>T
  hgvsp: ENST00000500065.4:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Cys221Cys
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

19-53612644-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612644
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612644
    reference: chr 19
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.615T>C
  hgvsp: ENST00000440291.1:c.615T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*695T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*530T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*530T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.798T>C
  hgvsp: ENST00000455735.2:c.798T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.690T>C
  hgvsp: ENST00000421033.1:c.690T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.-37T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.654T>C
  hgvsp: ENST00000243643.4:c.654T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.654T>C
  hgvsp: ENST00000500065.4:c.654T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.798T>C
  hgvsp: ENST00000448501.1:c.798T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*530T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*530T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*695T>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr218Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP

19-53612663-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612663
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612663
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*511G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.779G>C
  hgvsp: ENSP00000388787.2:p.Arg260Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.596G>C
  hgvsp: ENSP00000414601.1:p.Arg199Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*511G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*511G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.671G>C
  hgvsp: ENSP00000395055.1:p.Arg224Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*676G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.635G>C
  hgvsp: ENSP00000243643.3:p.Arg212Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.-56G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.779G>C
  hgvsp: ENSP00000396492.1:p.Arg260Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.635G>C
  hgvsp: ENSP00000439435.1:p.Arg212Thr
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*511G>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*676G>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg212Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

19-53612667-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612667
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612667
    reference: chr 19
allele count: 16
allele frequency: 1.317978879388458e-4
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.592A>G
  hgvsp: ENSP00000414601.1:p.Ile198Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.-60A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*507A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.631A>G
  hgvsp: ENSP00000439435.1:p.Ile211Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*507A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*507A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.631A>G
  hgvsp: ENSP00000243643.3:p.Ile211Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*672A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.775A>G
  hgvsp: ENSP00000388787.2:p.Ile259Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.667A>G
  hgvsp: ENSP00000395055.1:p.Ile223Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.775A>G
  hgvsp: ENSP00000396492.1:p.Ile259Val
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*672A>G
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*507A>G
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Ile211Val
num of homozygotes: 2
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

19-53612670-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612670
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612670
    reference: chr 19
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.589T>C
  hgvsp: ENSP00000414601.1:p.Cys197Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.628T>C
  hgvsp: ENSP00000439435.1:p.Cys210Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*504T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*504T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.772T>C
  hgvsp: ENSP00000396492.1:p.Cys258Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*504T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.628T>C
  hgvsp: ENSP00000243643.3:p.Cys210Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*669T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*504T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.772T>C
  hgvsp: ENSP00000388787.2:p.Cys258Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.664T>C
  hgvsp: ENSP00000395055.1:p.Cys222Arg
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.-63T>C
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*669T>C
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys210Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-53612683-TTGTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612683
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612679
    reference: chr 19
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*487_*490delCACA
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*652_*655delCACA
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*487_*490delCACA
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.611_614delCACA
  hgvsp: ENSP00000243643.3:p.Thr204LysfsTer21
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.-80_-77delCACA
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*487_*490delCACA
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.647_650delCACA
  hgvsp: ENSP00000395055.1:p.Thr216LysfsTer21
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.572_575delCACA
  hgvsp: ENSP00000414601.1:p.Thr191LysfsTer21
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*487_*490delCACA
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.755_758delCACA
  hgvsp: ENSP00000388787.2:p.Thr252LysfsTer21
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.755_758delCACA
  hgvsp: ENSP00000396492.1:p.Thr252LysfsTer21
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.611_614delCACA
  hgvsp: ENSP00000439435.1:p.Thr204LysfsTer21
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*652_*655delCACA
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5135
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr204LysfsTer21
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: TTGTG
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

19-53612685-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53612685
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 53612685
    reference: chr 19
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000243643
  ensembl transcript: ENST00000243643
  gene symbol: ZNF415
  hgvsc: ENST00000243643.4:c.613C>T
  hgvsp: ENSP00000243643.3:p.Gln205Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000396492
  ensembl transcript: ENST00000448501
  gene symbol: ZNF415
  hgvsc: ENST00000448501.1:c.757C>T
  hgvsp: ENSP00000396492.1:p.Gln253Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472911
  ensembl transcript: ENST00000601493
  gene symbol: ZNF415
  hgvsc: ENST00000601493.1:c.-78C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000414601
  ensembl transcript: ENST00000440291
  gene symbol: ZNF415
  hgvsc: ENST00000440291.1:c.574C>T
  hgvsp: ENSP00000414601.1:p.Gln192Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000471834
  ensembl transcript: ENST00000600120
  gene symbol: ZNF415
  hgvsc: ENST00000600120.1:c.*654C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000468917
  ensembl transcript: ENST00000597503
  gene symbol: ZNF415
  hgvsc: ENST00000597503.1:c.*489C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000395055
  ensembl transcript: ENST00000421033
  gene symbol: ZNF415
  hgvsc: ENST00000421033.1:c.649C>T
  hgvsp: ENSP00000395055.1:p.Gln217Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000469656
  ensembl transcript: ENST00000597748
  gene symbol: ZNF415
  hgvsc: ENST00000597748.1:c.*489C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000439435
  ensembl transcript: ENST00000500065
  gene symbol: ZNF415
  hgvsc: ENST00000500065.4:c.613C>T
  hgvsp: ENSP00000439435.1:p.Gln205Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472516
  ensembl transcript: ENST00000595193
  gene symbol: ZNF415
  hgvsc: ENST00000595193.1:c.*489C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472673
  ensembl transcript: ENST00000598578
  gene symbol: ZNF415
  hgvsc: ENST00000598578.1:c.*654C>T
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000388787
  ensembl transcript: ENST00000455735
  gene symbol: ZNF415
  hgvsc: ENST00000455735.2:c.757C>T
  hgvsp: ENSP00000388787.2:p.Gln253Ter
  variant of: http://identifiers.org/hgnc/20636
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000170954
  ensembl protein: ENSP00000472584
  ensembl transcript: ENST00000594011
  gene symbol: ZNF415
  hgvsc: ENST00000594011.1:c.*489C>T
  variant of: http://identifiers.org/hgnc/20636
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5564
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln205Ter
num of homozygotes: 0
population: Other
reference allele: G

GenotypeDepth
all individuals: 5038
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5807
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3318
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1496
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4222
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10818
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37345
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1499
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3242
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
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: 10404
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.561e0

DP
type: SiteQuality
SIO_000300: 3.079778e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

QD
type: SiteQuality
SIO_000300: 1.134e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e-1

GenotypeDepth
all individuals: 7381
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5597
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3318
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5806
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3187
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37345
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1865
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1512
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10816
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1994
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3263
bin: 6.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 3.576e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.080018e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: 5.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.07e-1

QD
type: SiteQuality
SIO_000300: 1.494e1

GenotypeDepth
all individuals: 769
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2197
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1497
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1030
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10798
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3256
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37343
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1993
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49667246237784e-5
allele num: 66716
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

DP
type: SiteQuality
SIO_000300: 3.080325e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

FS
type: SiteQuality
SIO_000300: 1.746e0

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.94e0

QD
type: SiteQuality
SIO_000300: 1.255e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

GenotypeDepth
all individuals: 4221
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5600
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3318
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3187
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1665
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37342
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2151
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10811
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3263
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

FS
type: SiteQuality
SIO_000300: 1.1134e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.449e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.398e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 3.080358e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

QD
type: SiteQuality
SIO_000300: 9.58e0

GenotypeDepth
all individuals: 5154
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7400
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5597
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1496
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2197
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10829
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3268
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 37345
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1995
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
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: 6612
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.069e0

MQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

DP
type: SiteQuality
SIO_000300: 3.080428e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

VQSLOD
type: SiteQuality
SIO_000300: 3.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.24e-1

QD
type: SiteQuality
SIO_000300: 1.576e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.523e0

GenotypeDepth
all individuals: 3187
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5597
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1866
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37347
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1998
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10819
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

FS
type: SiteQuality
SIO_000300: 2.169e0

VQSLOD
type: SiteQuality
SIO_000300: 2.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

DP
type: SiteQuality
SIO_000300: 3.080558e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.889e0

MQRankSum
type: SiteQuality
SIO_000300: -6.33e-1

QD
type: SiteQuality
SIO_000300: 1.323e1

GenotypeDepth
all individuals: 5807
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7401
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3187
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5154
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5597
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10822
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2146
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1868
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37348
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 3.080629e6

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.523e1

FS
type: SiteQuality
SIO_000300: 5.172e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.247e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeDepth
all individuals: 5807
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3318
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1496
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3188
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3267
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10821
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37347
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2147
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.388e0

QD
type: SiteQuality
SIO_000300: 1.256e1

FS
type: SiteQuality
SIO_000300: 1.547e0

VQSLOD
type: SiteQuality
SIO_000300: 7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.68e-1

DP
type: SiteQuality
SIO_000300: 3.08063e6

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

GenotypeDepth
all individuals: 5807
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5597
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 769
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5465
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3267
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10821
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2147
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37347
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 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: 10404
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.256e1

FS
type: SiteQuality
SIO_000300: 1.547e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.388e0

VQSLOD
type: SiteQuality
SIO_000300: 7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.52e-1

DP
type: SiteQuality
SIO_000300: 3.08063e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 4222
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2198
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5042
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5599
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 602
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3267
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37348
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10824
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.75e1
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: 10404
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.080696e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

QD
type: SiteQuality
SIO_000300: 1.241e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 8.8e-1

GenotypeDepth
all individuals: 5466
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1496
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3187
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4631
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10768
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1657
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3250
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2159
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37346
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

FS
type: SiteQuality
SIO_000300: 3.855e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

QD
type: SiteQuality
SIO_000300: 1.199e1

VQSLOD
type: SiteQuality
SIO_000300: 9.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.315e0

DP
type: SiteQuality
SIO_000300: 3.080402e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

GenotypeDepth
all individuals: 3318
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4630
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3187
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 769
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2198
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37350
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3249
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10701
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.822e0

FS
type: SiteQuality
SIO_000300: 6.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

QD
type: SiteQuality
SIO_000300: 1.245e1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 3.080267e6

GenotypeDepth
all individuals: 3187
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4222
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3318
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 770
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 602
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10703
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3249
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1655
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37348
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1871
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

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

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.707e0

QD
type: SiteQuality
SIO_000300: 1.802e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.116e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.356e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 8.149999999999999e-1

DP
type: SiteQuality
SIO_000300: 3.080233e6

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

GenotypeDepth
all individuals: 1496
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4222
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1032
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 770
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5154
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3242
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10677
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37352
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2150
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1990
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.424536307431204e-4
allele num: 16498
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 4
allele frequency: 3.844675124951942e-4
allele num: 10404
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.16e0

FS
type: SiteQuality
SIO_000300: 5.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

DP
type: SiteQuality
SIO_000300: 3.080749e6

QD
type: SiteQuality
SIO_000300: 1.299e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeDepth
all individuals: 3321
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 602
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2198
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5453
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5807
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10710
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37349
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3249
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1649
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 4
allele frequency: 4.622140050843541e-4
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

VQSLOD
type: SiteQuality
SIO_000300: 2.17e0

FS
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 3.080488e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-1

QD
type: SiteQuality
SIO_000300: 1.224e1

GenotypeDepth
all individuals: 770
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5448
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1032
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3323
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1653
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10712
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37354
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 1990
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3251
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.697518283179475e-4
allele num: 66728
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.413e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.32e0

VQSLOD
type: SiteQuality
SIO_000300: 6.06e0

DP
type: SiteQuality
SIO_000300: 3.080693e6

GenotypeDepth
all individuals: 3322
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1497
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5149
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5043
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1874
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10697
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37353
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1648
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3251
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

QD
type: SiteQuality
SIO_000300: 1.159e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

FS
type: SiteQuality
SIO_000300: 3.934e0

MQRankSum
type: SiteQuality
SIO_000300: 2.27e0

VQSLOD
type: SiteQuality
SIO_000300: -9.124e-1

DP
type: SiteQuality
SIO_000300: 3.080493e6

GenotypeDepth
all individuals: 4221
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2200
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3321
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5598
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5807
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10706
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3238
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37351
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.049e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.433e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.529e0

VQSLOD
type: SiteQuality
SIO_000300: 4.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.080613e6

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

GenotypeDepth
all individuals: 1497
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5043
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4640
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3245
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 9.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1876
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37352
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

DP
type: SiteQuality
SIO_000300: 3.080473e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

QD
type: SiteQuality
SIO_000300: 1.284e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.533e0

VQSLOD
type: SiteQuality
SIO_000300: 3.6e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.599e0

GenotypeDepth
all individuals: 3188
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 771
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5807
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3322
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2144
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10709
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37354
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.496133325340207e-5
allele num: 66724
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.978e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.179e0

MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

QD
type: SiteQuality
SIO_000300: 1.189e1

FS
type: SiteQuality
SIO_000300: 1.527e0

DP
type: SiteQuality
SIO_000300: 3.08079e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.04e-1

GenotypeDepth
all individuals: 1497
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3187
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3321
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5044
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37353
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1989
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3242
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10734
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1650
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.312e0

QD
type: SiteQuality
SIO_000300: 9.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.91e-1

FS
type: SiteQuality
SIO_000300: 6.464e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 3.08051e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 5044
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4222
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3187
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2198
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1497
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1874
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1988
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1649
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37351
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.506e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

FS
type: SiteQuality
SIO_000300: 2.755e0

VQSLOD
type: SiteQuality
SIO_000300: 2.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.68e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.120000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.080527e6

QD
type: SiteQuality
SIO_000300: 1.239e1

GenotypeDepth
all individuals: 4647
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1497
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1033
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5045
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3226
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10693
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2143
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37353
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 5
allele frequency: 4.804920238324044e-4
allele num: 10406
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
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: 66722
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.285e1

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.26e0

DP
type: SiteQuality
SIO_000300: 3.081122e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

GenotypeDepth
all individuals: 1497
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 4640
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1035
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 3185
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3325
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10731
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1873
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3249
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37351
bin: 9.75e1
variant carriers: 20

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

African
type: Population
allele count: 7
allele frequency: 6.726888333653661e-4
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.348799568384138e-4
allele num: 66726
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.28e-1

DP
type: SiteQuality
SIO_000300: 3.081106e6

QD
type: SiteQuality
SIO_000300: 1.339e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 774
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3323
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3185
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1033
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5045
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1663
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37358
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1878
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3242
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10764
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 3.08138e6

QD
type: SiteQuality
SIO_000300: 1.277e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.35e-1

FS
type: SiteQuality
SIO_000300: 2.011e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.08e-1

GenotypeDepth
all individuals: 4681
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3186
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5045
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4219
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 37359
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3232
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1657
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2146
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1879
bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.365e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.104e0

DP
type: SiteQuality
SIO_000300: 3.08162e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.963e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.737e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.467e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

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

GenotypeDepth
all individuals: 3186
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1032
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1496
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4645
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10788
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1510
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1879
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3233
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37366
bin: 9.75e1
variant carriers: 8

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

African
type: Population
allele count: 5
allele frequency: 4.804920238324044e-4
allele num: 10406
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.592016588906169e-4
allele num: 11574
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.951e1

QD
type: SiteQuality
SIO_000300: 1.345e1

DP
type: SiteQuality
SIO_000300: 3.081846e6

FS
type: SiteQuality
SIO_000300: 1.104e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.58e-1

GenotypeDepth
all individuals: 774
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 603
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3187
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5045
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1496
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1666
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1882
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2144
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10804
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3225
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37364
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.082047e6

MQRankSum
type: SiteQuality
SIO_000300: -9.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.089e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.326e0

QD
type: SiteQuality
SIO_000300: 1.219e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.754e0

GenotypeDepth
all individuals: 1059
bin: 8.25e1
variant carriers: 34

GenotypeDepth
all individuals: 4236
bin: 6.25e1
variant carriers: 35

GenotypeDepth
all individuals: 786
bin: 8.75e1
variant carriers: 18

GenotypeDepth
all individuals: 5813
bin: 5.25e1
variant carriers: 41

GenotypeDepth
all individuals: 4621
bin: 3.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1639
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3186
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1872
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10746
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2125
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37586
bin: 9.75e1
variant carriers: 461

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

South Asian
type: Population
allele count: 8
allele frequency: 4.845548152634767e-4
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.637070305752289e-4
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 398
allele frequency: 5.964333882811329e-3
allele num: 66730
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 38
allele frequency: 5.745388569700635e-3
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
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: 7
allele frequency: 7.709251101321586e-3
allele num: 908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.38e-1

FS
type: SiteQuality
SIO_000300: 5.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

QD
type: SiteQuality
SIO_000300: 1.523e1

DP
type: SiteQuality
SIO_000300: 3.095458e6

GenotypeDepth
all individuals: 4641
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4654
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4241
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 775
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1880
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10862
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37362
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1516
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817300702689605e-4
allele num: 16508
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

FS
type: SiteQuality
SIO_000300: 3.529e0

DP
type: SiteQuality
SIO_000300: 3.084295e6

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

QD
type: SiteQuality
SIO_000300: 1.317e1

GenotypeDepth
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2215
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1040
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4239
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3195
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10875
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1974
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37363
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1883
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3234
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2135
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
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: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.384e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

DP
type: SiteQuality
SIO_000300: 3.084267e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
SIO_000300: 7.593e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.96e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.79e0

GenotypeDepth
all individuals: 1039
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 776
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5156
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5793
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4237
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37364
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3230
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1643
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10874
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1517
bin: 8.75e1
variant carriers: 0

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

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

European (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: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495594317568783e-5
allele num: 66732
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e-1

QD
type: SiteQuality
SIO_000300: 1.317e1

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 3.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.94e1

DP
type: SiteQuality
SIO_000300: 3.084455e6

MQRankSum
type: SiteQuality
SIO_000300: -6.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.27e-1

GenotypeDepth
all individuals: 7436
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 776
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3330
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 604
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5027
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3234
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1883
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37369
bin: 9.75e1
variant carriers: 11

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

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10858
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.198861081972126e-4
allele num: 66730
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

FS
type: SiteQuality
SIO_000300: 1.747e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.369e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-2

DP
type: SiteQuality
SIO_000300: 3.085074e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeDepth
all individuals: 615
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1047
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5149
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5037
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 778
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2123
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10821
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1874
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37470
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 1

South Asian
type: Population
allele count: 10
allele frequency: 6.05766900896535e-4
allele num: 16508
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

DP
type: SiteQuality
SIO_000300: 3.090905e6

QD
type: SiteQuality
SIO_000300: 1.274e1

FS
type: SiteQuality
SIO_000300: 5.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.29e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e-1

GenotypeDepth
all individuals: 3352
bin: 9.75e1
variant carriers: 23

GenotypeDepth
all individuals: 4627
bin: 3.75e1
variant carriers: 3

GenotypeDepth
all individuals: 5444
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2238
bin: 7.25e1
variant carriers: 22

GenotypeDepth
all individuals: 778
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 10821
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37470
bin: 9.75e1
variant carriers: 178

GenotypeQuality
all individuals: 2123
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1628
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1874
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 99
allele frequency: 1.483501663320047e-3
allele num: 66734
num of homozygotes: 0

South Asian
type: Population
allele count: 69
allele frequency: 4.179791616186091e-3
allele num: 16508
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.047777441790142e-4
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.184033177812338e-4
allele num: 11574
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.39e-1

DP
type: SiteQuality
SIO_000300: 3.090905e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e0

QD
type: SiteQuality
SIO_000300: 1.274e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.29e-2

FS
type: SiteQuality
SIO_000300: 5.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeDepth
all individuals: 5154
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5790
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5034
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3200
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2222
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1876
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37377
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10874
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3235
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1512
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.08647e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.382e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

GenotypeDepth
all individuals: 5033
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4629
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7452
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37378
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3235
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1512
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10879
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1977
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2133
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1879
bin: 8.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 66730
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.065e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 6.614e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.857e0

MQRankSum
type: SiteQuality
SIO_000300: -8.75e-1

QD
type: SiteQuality
SIO_000300: 1.719e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.086442e6

GenotypeDepth
all individuals: 7450
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4248
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1509
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5033
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 771
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37378
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10902
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3235
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1977
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1878
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.17e0

DP
type: SiteQuality
SIO_000300: 3.086508e6

FS
type: SiteQuality
SIO_000300: 2.359e0

MQRankSum
type: SiteQuality
SIO_000300: 6.22e-1

QD
type: SiteQuality
SIO_000300: 1.266e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

MQ
type: SiteQuality
SIO_000300: 5.93e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.68e-1

GenotypeDepth
all individuals: 608
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7440
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1509
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5149
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 771
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10881
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37385
bin: 9.75e1
variant carriers: 12

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1881
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2133
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3238
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

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

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: 12
allele frequency: 1.798129944857348e-4
allele num: 66736
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

FS
type: SiteQuality
SIO_000300: 1.108e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.661e0

DP
type: SiteQuality
SIO_000300: 3.087142e6

QD
type: SiteQuality
SIO_000300: 1.256e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

GenotypeDepth
all individuals: 1064
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2237
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3357
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 617
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4275
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10776
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37173
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3188
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1492
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2098
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1845
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1613
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.199904007679386e-4
allele num: 66672
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 3.64e-1

QD
type: SiteQuality
SIO_000300: 1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.38e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.35237e2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.581e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.58e-1

DP
type: SiteQuality
SIO_000300: 3.095785e6

GenotypeDepth
all individuals: 1056
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4583
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5465
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5138
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2234
bin: 7.25e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 10898
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3221
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1866
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37475
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1619
bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.492208103572285e-5
allele num: 66736
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: 11576
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 3.091524e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

FS
type: SiteQuality
SIO_000300: 3.292e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.641e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

GenotypeDepth
all individuals: 613
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1056
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5040
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2232
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 779
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1868
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3221
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 37471
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10902
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 7.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 66736
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.091416e6

VQSLOD
type: SiteQuality
SIO_000300: -1.113e0

MQRankSum
type: SiteQuality
SIO_000300: -7.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.74e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 8.407999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.93e0

GenotypeDepth
all individuals: 5572
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5783
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4624
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3344
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 613
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37470
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1622
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10899
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.294e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.34e-1

DP
type: SiteQuality
SIO_000300: 3.091395e6

VQSLOD
type: SiteQuality
SIO_000300: 6.64e-1

FS
type: SiteQuality
SIO_000300: 1.205e0

QD
type: SiteQuality
SIO_000300: 1.422e1

GenotypeDepth
all individuals: 782
bin: 8.75e1
variant carriers: 3

GenotypeDepth
all individuals: 1058
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 5781
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5464
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3350
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 37476
bin: 9.75e1
variant carriers: 23

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10902
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3222
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

East Asian
type: Population
allele count: 22
allele frequency: 2.542177027963947e-3
allele num: 8654
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.28e0

VQSLOD
type: SiteQuality
SIO_000300: 5.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.346e1

DP
type: SiteQuality
SIO_000300: 3.092024e6

GenotypeDepth
all individuals: 781
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1529
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5569
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5136
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3347
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1621
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10898
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3224
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1503
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37476
bin: 9.75e1
variant carriers: 1

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

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

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

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: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.682e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.653e0

VQSLOD
type: SiteQuality
SIO_000300: -1.287e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.32e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.1988e1

DP
type: SiteQuality
SIO_000300: 3.091972e6

GenotypeDepth
all individuals: 781
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3348
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7448
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5037
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1059
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10891
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3224
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37475
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1964
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1503
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

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

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

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

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: 16506
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.658e0

MQRankSum
type: SiteQuality
SIO_000300: -2.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.979e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.67e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-2

DP
type: SiteQuality
SIO_000300: 3.092023e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

GenotypeDepth
all individuals: 613
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5469
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4579
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1529
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5569
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3225
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37476
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1868
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10896
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

QD
type: SiteQuality
SIO_000300: 1.897e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 3.092034e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

GenotypeDepth
all individuals: 7433
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 613
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1529
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4568
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3221
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1620
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10869
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37476
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1867
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.08e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

FS
type: SiteQuality
SIO_000300: 4.627e0

VQSLOD
type: SiteQuality
SIO_000300: -2.097e0

DP
type: SiteQuality
SIO_000300: 3.092007e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.437e0

QD
type: SiteQuality
SIO_000300: 1.539e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

GenotypeDepth
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5780
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 613
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5037
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4260
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1503
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1867
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3222
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37477
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10865
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.02e0

QD
type: SiteQuality
SIO_000300: 1.439e1

MQRankSum
type: SiteQuality
SIO_000300: -1.757e0

VQSLOD
type: SiteQuality
SIO_000300: -8.314e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.084e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.319e0

DP
type: SiteQuality
SIO_000300: 3.091984e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.18e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeDepth
all individuals: 3350
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 613
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5037
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3219
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1529
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3219
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1623
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10871
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1866
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37478
bin: 9.75e1
variant carriers: 2

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.092112e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.634e0

MQRankSum
type: SiteQuality
SIO_000300: -1.518e0

VQSLOD
type: SiteQuality
SIO_000300: 7.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

FS
type: SiteQuality
SIO_000300: 3.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.21e-2

QD
type: SiteQuality
SIO_000300: 1.34e1

GenotypeDepth
all individuals: 5569
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1529
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 613
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 781
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3349
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3220
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10872
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37477
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1866
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.515e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 4.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
SIO_000300: 7.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e0

DP
type: SiteQuality
SIO_000300: 3.09212e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.328e0

GenotypeDepth
all individuals: 4625
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5033
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2233
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 783
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3372
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37485
bin: 9.75e1
variant carriers: 29

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10864
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3216
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1620
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 26
allele frequency: 3.004391033048301e-3
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.352e1

FS
type: SiteQuality
SIO_000300: 5.37e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

DP
type: SiteQuality
SIO_000300: 3.093792e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.357e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.04e0

GenotypeDepth
all individuals: 5779
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4624
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5136
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3360
bin: 9.75e1
variant carriers: 6

GenotypeDepth
all individuals: 783
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37480
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3216
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10860
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1620
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 7.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 9
allele frequency: 8.650519031141869e-4
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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.55e0

QD
type: SiteQuality
SIO_000300: 1.495e1

FS
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.46e-2

DP
type: SiteQuality
SIO_000300: 3.093209e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeDepth
all individuals: 4626
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5776
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 784
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3370
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10867
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3216
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37481
bin: 9.75e1
variant carriers: 1

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.763e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e0

MQRankSum
type: SiteQuality
SIO_000300: 6.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 3.093717e6

GenotypeDepth
all individuals: 4255
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4626
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1062
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 784
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10867
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3216
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37481
bin: 9.75e1
variant carriers: 12

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

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

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

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 11
allele frequency: 9.500777336327518e-4
allele num: 11578
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.763e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

DP
type: SiteQuality
SIO_000300: 3.093717e6

GenotypeDepth
all individuals: 1530
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5031
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3368
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2233
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10857
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3213
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37478
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.264e1

VQSLOD
type: SiteQuality
SIO_000300: -1.315e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.55e-1

DP
type: SiteQuality
SIO_000300: 3.093479e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.14e-1

GenotypeDepth
all individuals: 5453
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5030
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1066
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 618
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 787
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1962
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10839
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1859
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1619
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37508
bin: 9.75e1
variant carriers: 50

African
type: Population
allele count: 50
allele frequency: 4.805843906189927e-3
allele num: 10404
num of homozygotes: 0

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

MQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

DP
type: SiteQuality
SIO_000300: 3.097122e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 1.342e1

GenotypeDepth
all individuals: 1532
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2234
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4252
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3215
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1613
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37510
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2108
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1868
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.174e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.259e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 3.095444e6

GenotypeDepth
all individuals: 3214
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5445
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5033
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7363
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1532
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37512
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2103
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10743
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3200
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 9.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997332374186974e-5
allele num: 66726
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.19e-1

QD
type: SiteQuality
SIO_000300: 1.134e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

DP
type: SiteQuality
SIO_000300: 3.095725e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

GenotypeDepth
all individuals: 5562
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2234
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5132
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3201
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37512
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 10744
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1963
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 5.19e-1

DP
type: SiteQuality
SIO_000300: 3.09595e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.025e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.941e1

QD
type: SiteQuality
SIO_000300: 1.131e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.56e-1

GenotypeDepth
all individuals: 786
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1535
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3386
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7376
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2235
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10770
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1616
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2109
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37519
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1500
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3208
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
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: 66734
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.04e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

VQSLOD
type: SiteQuality
SIO_000300: 3.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.074e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.26e-1

QD
type: SiteQuality
SIO_000300: 1.401e1

DP
type: SiteQuality
SIO_000300: 3.096007e6

GenotypeDepth
all individuals: 5777
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3215
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 786
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5478
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1535
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37520
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10776
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1618
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1881
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2121
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3213
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 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: 10404
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: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
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: 66734
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.096539e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.896e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

FS
type: SiteQuality
SIO_000300: 2.743e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.87e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

QD
type: SiteQuality
SIO_000300: 1.11e1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e-1

GenotypeDepth
all individuals: 788
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1536
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 622
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7390
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5776
bin: 5.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1881
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3216
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37527
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 1504
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
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: 15
allele frequency: 9.087604507451836e-4
allele num: 16506
num of homozygotes: 2

MQ
type: SiteQuality
SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.51e-2

DP
type: SiteQuality
SIO_000300: 3.09704e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-2

QD
type: SiteQuality
SIO_000300: 1.594e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.38e-1

GenotypeDepth
all individuals: 621
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5776
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3387
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3216
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1624
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37525
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10785
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1885
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2127
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.49e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

DP
type: SiteQuality
SIO_000300: 3.096882e6

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

QD
type: SiteQuality
SIO_000300: 1.158e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.194e0

GenotypeDepth
all individuals: 1073
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3388
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5562
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3216
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2234
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1625
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37525
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3231
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10784
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2130
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
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 (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.275e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.871e0

DP
type: SiteQuality
SIO_000300: 3.097336e6

QD
type: SiteQuality
SIO_000300: 9.279999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.232e0

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.63e1

GenotypeDepth
all individuals: 5030
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3387
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5776
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4633
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1889
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10784
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1624
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3232
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37525
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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