X-106186305-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186305
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186305
    reference: chr 0
allele count: 3
allele frequency: 3.419933653287126e-5
allele num: 87721
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1816C>A
  hgvsp: ENSP00000347821.4:p.Pro606Thr
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.1060C>A
  hgvsp: ENSP00000440359.1:p.Pro354Thr
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50155C>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1816C>A
  hgvsp: ENSP00000255495.7:p.Pro606Thr
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
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genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro606Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

X-106186310-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186310
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186310
    reference: chr 0
allele count: 1
allele frequency: 1.140003876013178e-5
allele num: 87719
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1811C>T
  hgvsp: ENSP00000255495.7:p.Ala604Val
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.1055C>T
  hgvsp: ENSP00000440359.1:p.Ala352Val
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1811C>T
  hgvsp: ENSP00000347821.4:p.Ala604Val
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50150C>T
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 171
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6
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genotype quality: GenotypeQuality
  all individuals: 13
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala604Val
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

X-106186314-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186314
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186314
    reference: chr 0
allele count: 14
allele frequency: 1.596023621149593e-4
allele num: 87718
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.1051G>C
  hgvsp: ENSP00000440359.1:p.Val351Leu
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1807G>C
  hgvsp: ENSP00000347821.4:p.Val603Leu
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1807G>C
  hgvsp: ENSP00000255495.7:p.Val603Leu
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50146G>C
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6513
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genotype quality: GenotypeQuality
  all individuals: 7302
  bin: 9.75e1
  variant carriers: 14
hgvs: p.Val603Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-106186314-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186314
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186314
    reference: chr 0
allele count: 2
allele frequency: 2.280033744499419e-5
allele num: 87718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50146G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1807G>A
  hgvsp: ENSP00000255495.7:p.Val603Ile
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.1051G>A
  hgvsp: ENSP00000440359.1:p.Val351Ile
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1807G>A
  hgvsp: ENSP00000347821.4:p.Val603Ile
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val603Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-106186339-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186339
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186339
    reference: chr 0
allele count: 1
allele frequency: 1.140432908332003e-5
allele num: 87686
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.1026T>C
  hgvsp: ENST00000535534.1:c.1026T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1782T>C
  hgvsp: ENST00000355610.4:c.1782T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50121T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1782T>C
  hgvsp: ENST00000255495.7:c.1782T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2825
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36966
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1660
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 1864
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7286
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2367
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala594Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

X-106186341-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186341
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186341
    reference: chr 0
allele count: 1
allele frequency: 1.140484934194019e-5
allele num: 87682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50119G>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1780G>T
  hgvsp: ENSP00000347821.4:p.Ala594Ser
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1780G>T
  hgvsp: ENSP00000255495.7:p.Ala594Ser
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.1024G>T
  hgvsp: ENSP00000440359.1:p.Ala342Ser
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12441
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 10
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala594Ser
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

X-106186347-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186347
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186347
    reference: chr 0
allele count: 1
allele frequency: 1.14073212187582e-5
allele num: 87663
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.1018A>G
  hgvsp: ENSP00000440359.1:p.Met340Val
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1774A>G
  hgvsp: ENSP00000255495.7:p.Met592Val
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1774A>G
  hgvsp: ENSP00000347821.4:p.Met592Val
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50113A>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12425
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11155
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2825
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genotype quality: GenotypeQuality
  all individuals: 8
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genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
hgvs: p.Met592Val
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

X-106186349-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186349
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186349
    reference: chr 0
allele count: 1
allele frequency: 1.140901312036509e-5
allele num: 87650
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50111C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1772C>G
  hgvsp: ENSP00000347821.4:p.Ser591Cys
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1772C>G
  hgvsp: ENSP00000255495.7:p.Ser591Cys
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.1016C>G
  hgvsp: ENSP00000440359.1:p.Ser339Cys
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 5.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21003
  bin: 2.75e1
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genotype depth: GenotypeDepth
  all individuals: 80
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2367
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2825
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser591Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS

X-106186355-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186355
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186355
    reference: chr 0
allele count: 2
allele frequency: 2.282245272899479e-5
allele num: 87633
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.1010A>G
  hgvsp: ENSP00000440359.1:p.Asp337Gly
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1766A>G
  hgvsp: ENSP00000347821.4:p.Asp589Gly
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50105A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1766A>G
  hgvsp: ENSP00000255495.7:p.Asp589Gly
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20991
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36897
  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp589Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

X-106186359-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186359
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186359
    reference: chr 0
allele count: 1
allele frequency: 1.141344046749452e-5
allele num: 87616
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1762C>G
  hgvsp: ENSP00000347821.4:p.Leu588Val
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.1006C>G
  hgvsp: ENSP00000440359.1:p.Leu336Val
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1762C>G
  hgvsp: ENSP00000255495.7:p.Leu588Val
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50101C>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6490
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  variant carriers: 0
hgvs: p.Leu588Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

X-106186365-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186365
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186365
    reference: chr 0
allele count: 5
allele frequency: 5.711609417301607e-5
allele num: 87541
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1756C>T
  hgvsp: ENSP00000347821.4:p.Pro586Ser
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.1000C>T
  hgvsp: ENSP00000440359.1:p.Pro334Ser
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1756C>T
  hgvsp: ENSP00000255495.7:p.Pro586Ser
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50095C>T
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 7.75e1
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hgvs: p.Pro586Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum

X-106186368-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186368
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186368
    reference: chr 0
allele count: 1
allele frequency: 1.142883265903221e-5
allele num: 87498
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.997A>C
  hgvsp: ENSP00000440359.1:p.Thr333Pro
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1753A>C
  hgvsp: ENSP00000347821.4:p.Thr585Pro
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1753A>C
  hgvsp: ENSP00000255495.7:p.Thr585Pro
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50092A>C
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 385
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genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 36
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genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr585Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

X-106186381-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186381
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186381
    reference: chr 0
allele count: 5
allele frequency: 5.739342041828325e-5
allele num: 87118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1740G>T
  hgvsp: ENSP00000255495.7:p.Gln580His
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50079G>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.984G>T
  hgvsp: ENSP00000440359.1:p.Gln328His
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1740G>T
  hgvsp: ENSP00000347821.4:p.Gln580His
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
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genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35830
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln580His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

X-106186405-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186405
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186405
    reference: chr 0
allele count: 5
allele frequency: 5.812534148638124e-5
allele num: 86021
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50055G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.960G>A
  hgvsp: ENST00000535534.1:c.960G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1716G>A
  hgvsp: ENST00000355610.4:c.1716G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1716G>A
  hgvsp: ENST00000255495.7:c.1716G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1805
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33986
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  variant carriers: 1
hgvs: p.Pro572Pro
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

X-106186420-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186420
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186420
    reference: chr 0
allele count: 9
allele frequency: 1.057144535150056e-4
allele num: 85135
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.945C>T
  hgvsp: ENST00000535534.1:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50040C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1701C>T
  hgvsp: ENST00000355610.4:c.1701C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1701C>T
  hgvsp: ENST00000255495.7:c.1701C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3647
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  variant carriers: 0
hgvs: p.Ile567Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ

X-106186428-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186428
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186428
    reference: chr 0
allele count: 23
allele frequency: 2.723472783033949e-4
allele num: 84451
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1693A>G
  hgvsp: ENSP00000255495.7:p.Lys565Glu
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.937A>G
  hgvsp: ENSP00000440359.1:p.Lys313Glu
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50032A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1693A>G
  hgvsp: ENSP00000347821.4:p.Lys565Glu
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 78
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4204
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
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  variant carriers: 0
hgvs: p.Lys565Glu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

X-106186430-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186430
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186430
    reference: chr 0
allele count: 2
allele frequency: 2.371241582092384e-5
allele num: 84344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.935A>T
  hgvsp: ENSP00000440359.1:p.Tyr312Phe
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1691A>T
  hgvsp: ENSP00000255495.7:p.Tyr564Phe
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1691A>T
  hgvsp: ENSP00000347821.4:p.Tyr564Phe
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50030A>T
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32134
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7263
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5942
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2776
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2343
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4277
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr564Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

X-106186438-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186438
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186438
    reference: chr 0
allele count: 1
allele frequency: 1.200927115733346e-5
allele num: 83269
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.930-3C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1686-3C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50022C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1686-3C>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10514
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 616
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genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 4.75e1
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genotype depth: GenotypeDepth
  all individuals: 920
  bin: 2.5e0
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genotype depth: GenotypeDepth
  all individuals: 385
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2756
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 306
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genotype quality: GenotypeQuality
  all individuals: 31003
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7261
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 168
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genotype quality: GenotypeQuality
  all individuals: 276
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genotype quality: GenotypeQuality
  all individuals: 4743
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 973
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5847
  bin: 6.75e1
  variant carriers: 0
hgvs: c.1686-3C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS

X-106186439-CAAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186439
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186436
    reference: chr 0
allele count: 1
allele frequency: 1.202197617244323e-5
allele num: 83181
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1686-7_1686-5delCTT
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50018_111+50020delCTT
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.930-7_930-5delCTT
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1686-7_1686-5delCTT
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5124
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9022
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 922
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 100
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genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 96
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1065
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
hgvs: c.1686-7_1686-5delCTT
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: CAAG
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

X-106186459-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186459
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186459
    reference: chr 0
allele count: 2
allele frequency: 2.469288227668375e-5
allele num: 80995
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.930-24C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1686-24C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1686-24C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+50001C>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16224
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 903
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9809
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
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genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1492
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genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7257
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-106186469-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186469
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186469
    reference: chr 0
allele count: 13
allele frequency: 1.629889669007021e-4
allele num: 79760
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1686-34T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+49991T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.930-34T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1686-34T>C
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.5e0
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genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 4.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 534
  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 7251
  bin: 9.75e1
  variant carriers: 11
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-106186473-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106186473
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106186473
    reference: chr 0
allele count: 1
allele frequency: 1.262259697310125e-5
allele num: 79223
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+49987A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1686-38A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1686-38A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.930-38A>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2283
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7241
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

X-106198111-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198111
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198111
    reference: chr 0
allele count: 6
allele frequency: 6.843534000958095e-5
allele num: 87674
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1685+32T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1685+32T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38349T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.929+32T>C
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10224
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
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  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

X-106198115-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198115
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198115
    reference: chr 0
allele count: 7
allele frequency: 7.983485589808511e-5
allele num: 87681
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.929+28A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38345A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1685+28A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1685+28A>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 201
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genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 465
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

X-106198122-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198122
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198122
    reference: chr 0
allele count: 1
allele frequency: 1.140211851361983e-5
allele num: 87703
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38338C>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.929+21C>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1685+21C>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1685+21C>A
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
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  bin: 1.75e1
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genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 9.75e1
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genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 464
  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

X-106198129-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198129
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198129
    reference: chr 0
allele count: 1
allele frequency: 1.140016872249709e-5
allele num: 87718
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1685+14A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1685+14A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.929+14A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38331A>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-106198135-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198135
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198135
    reference: chr 0
allele count: 5
allele frequency: 5.699434616086084e-5
allele num: 87728
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38325A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1685+8A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1685+8A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.929+8A>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10420
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genotype depth: GenotypeDepth
  all individuals: 270
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 118
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
hgvs: c.1685+8A>G
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

X-106198137-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198137
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198137
    reference: chr 0
allele count: 29
allele frequency: 3.305559038424274e-4
allele num: 87731
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.929+6T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1685+6T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38323T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1685+6T>C
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
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  variant carriers: 0
hgvs: c.1685+6T>C
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

X-106198138-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198138
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198138
    reference: chr 0
allele count: 1
allele frequency: 1.139795976520203e-5
allele num: 87735
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1685+5C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1685+5C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38322C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.929+5C>T
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: c.1685+5C>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

X-106198139-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198139
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198139
    reference: chr 0
allele count: 11
allele frequency: 1.25374699385664e-4
allele num: 87737
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1685+4A>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.929+4A>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1685+4A>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38321A>T
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2010
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 462
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  variant carriers: 0
hgvs: c.1685+4A>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD

X-106198141-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198141
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198141
    reference: chr 0
allele count: 1
allele frequency: 1.139718033758448e-5
allele num: 87741
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1685+2T>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.929+2T>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1685+2T>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38319T>A
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12444
  bin: 3.25e1
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genotype depth: GenotypeDepth
  all individuals: 398
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.1685+2T>A
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

X-106198144-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198144
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198144
    reference: chr 0
allele count: 2
allele frequency: 2.279358132749818e-5
allele num: 87744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1684A>G
  hgvsp: ENSP00000255495.7:p.Ser562Gly
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38316A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.928A>G
  hgvsp: ENSP00000440359.1:p.Ser310Gly
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1684A>G
  hgvsp: ENSP00000347821.4:p.Ser562Gly
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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genotype depth: GenotypeDepth
  all individuals: 545
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
hgvs: p.Ser562Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

X-106198145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198145
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198145
    reference: chr 0
allele count: 1
allele frequency: 1.139653089599526e-5
allele num: 87746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38315C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1683C>T
  hgvsp: ENST00000355610.4:c.1683C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1683C>T
  hgvsp: ENST00000255495.7:c.1683C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.927C>T
  hgvsp: ENST00000535534.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1829
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hgvs: c.1683C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

X-106198146-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198146
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198146
    reference: chr 0
allele count: 1
allele frequency: 1.139692055206683e-5
allele num: 87743
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.926C>T
  hgvsp: ENSP00000440359.1:p.Ser309Phe
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38314C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1682C>T
  hgvsp: ENSP00000347821.4:p.Ser561Phe
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1682C>T
  hgvsp: ENSP00000255495.7:p.Ser561Phe
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1
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hgvs: p.Ser561Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

X-106198152-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198152
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198152
    reference: chr 0
allele count: 1
allele frequency: 1.139562180210363e-5
allele num: 87753
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.920A>T
  hgvsp: ENSP00000440359.1:p.Gln307Leu
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1676A>T
  hgvsp: ENSP00000347821.4:p.Gln559Leu
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1676A>T
  hgvsp: ENSP00000255495.7:p.Gln559Leu
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38308A>T
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12448
  bin: 3.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Gln559Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-106198174-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198174
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198174
    reference: chr 0
allele count: 1
allele frequency: 1.139458301523456e-5
allele num: 87761
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38286C>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1654C>A
  hgvsp: ENSP00000255495.7:p.Pro552Thr
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.898C>A
  hgvsp: ENSP00000440359.1:p.Pro300Thr
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1654C>A
  hgvsp: ENSP00000347821.4:p.Pro552Thr
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Pro552Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

X-106198185-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198185
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198185
    reference: chr 0
allele count: 1
allele frequency: 1.139458301523456e-5
allele num: 87761
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.887T>A
  hgvsp: ENSP00000440359.1:p.Leu296His
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38275T>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1643T>A
  hgvsp: ENSP00000255495.7:p.Leu548His
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1643T>A
  hgvsp: ENSP00000347821.4:p.Leu548His
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 545
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genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
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genotype depth: GenotypeDepth
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  bin: 7.5e0
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genotype depth: GenotypeDepth
  all individuals: 143
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genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
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genotype depth: GenotypeDepth
  all individuals: 31401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 2010
  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 42365
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 1827
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu548His
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

X-106198190-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198190
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198190
    reference: chr 0
allele count: 1
allele frequency: 1.139497253811618e-5
allele num: 87758
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1638A>G
  hgvsp: ENST00000355610.4:c.1638A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1638A>G
  hgvsp: ENST00000255495.7:c.1638A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.882A>G
  hgvsp: ENST00000535534.1:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38270A>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31405
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 42371
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genotype quality: GenotypeQuality
  all individuals: 566
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro546Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

X-106198207-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198207
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198207
    reference: chr 0
allele count: 1
allele frequency: 1.139536208763033e-5
allele num: 87755
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.865G>C
  hgvsp: ENSP00000440359.1:p.Glu289Gln
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1621G>C
  hgvsp: ENSP00000255495.7:p.Glu541Gln
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1621G>C
  hgvsp: ENSP00000347821.4:p.Glu541Gln
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38253G>C
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
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genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 463
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3
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genotype quality: GenotypeQuality
  all individuals: 42371
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genotype quality: GenotypeQuality
  all individuals: 1825
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu541Gln
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

X-106198219-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198219
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198219
    reference: chr 0
allele count: 1
allele frequency: 1.139640101655897e-5
allele num: 87747
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38241C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1609C>G
  hgvsp: ENSP00000255495.7:p.Pro537Ala
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.853C>G
  hgvsp: ENSP00000440359.1:p.Pro285Ala
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1609C>G
  hgvsp: ENSP00000347821.4:p.Pro537Ala
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
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genotype depth: GenotypeDepth
  all individuals: 142
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 10437
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genotype depth: GenotypeDepth
  all individuals: 399
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12446
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 950
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genotype depth: GenotypeDepth
  all individuals: 2258
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 180
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1822
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genotype quality: GenotypeQuality
  all individuals: 464
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genotype quality: GenotypeQuality
  all individuals: 566
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro537Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

X-106198226-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198226
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198226
    reference: chr 0
allele count: 1
allele frequency: 1.139640101655897e-5
allele num: 87747
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.846T>C
  hgvsp: ENST00000535534.1:c.846T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1602T>C
  hgvsp: ENST00000255495.7:c.1602T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38234T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1602T>C
  hgvsp: ENST00000355610.4:c.1602T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 9
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genotype quality: GenotypeQuality
  all individuals: 1822
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42355
  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2007
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 462
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser534Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

X-106198227-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198227
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198227
    reference: chr 0
allele count: 1
allele frequency: 1.139692055206683e-5
allele num: 87743
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38233G>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1601G>T
  hgvsp: ENSP00000255495.7:p.Ser534Ile
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.845G>T
  hgvsp: ENSP00000440359.1:p.Ser282Ile
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1601G>T
  hgvsp: ENSP00000347821.4:p.Ser534Ile
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 8223
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser534Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

X-106198229-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198229
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198229
    reference: chr 0
allele count: 1
allele frequency: 1.139692055206683e-5
allele num: 87743
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1599T>C
  hgvsp: ENST00000255495.7:c.1599T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1599T>C
  hgvsp: ENST00000355610.4:c.1599T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.843T>C
  hgvsp: ENST00000535534.1:c.843T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38231T>C
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 398
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 131
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5
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  variant carriers: 0
hgvs: p.Pro533Pro
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

X-106198259-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198259
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198259
    reference: chr 0
allele count: 1
allele frequency: 1.141265892127548e-5
allele num: 87622
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1569G>C
  hgvsp: ENSP00000347821.4:p.Lys523Asn
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1569G>C
  hgvsp: ENSP00000255495.7:p.Lys523Asn
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.813G>C
  hgvsp: ENSP00000440359.1:p.Lys271Asn
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38201G>C
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 26
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genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys523Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

X-106198260-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198260
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198260
    reference: chr 0
allele count: 1
allele frequency: 1.141396155777747e-5
allele num: 87612
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38200A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1568A>G
  hgvsp: ENSP00000347821.4:p.Lys523Arg
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1568A>G
  hgvsp: ENSP00000255495.7:p.Lys523Arg
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.812A>G
  hgvsp: ENSP00000440359.1:p.Lys271Arg
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Lys523Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

X-106198276-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198276
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198276
    reference: chr 0
allele count: 6
allele frequency: 6.874190850451978e-5
allele num: 87283
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38184G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1552G>A
  hgvsp: ENSP00000255495.7:p.Ala518Thr
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1552G>A
  hgvsp: ENSP00000347821.4:p.Ala518Thr
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.796G>A
  hgvsp: ENSP00000440359.1:p.Ala266Thr
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ala518Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

X-106198300-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198300
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198300
    reference: chr 0
allele count: 1
allele frequency: 1.170864214877001e-5
allele num: 85407
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.772A>G
  hgvsp: ENSP00000440359.1:p.Lys258Glu
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1528A>G
  hgvsp: ENSP00000255495.7:p.Lys510Glu
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38160A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1528A>G
  hgvsp: ENSP00000347821.4:p.Lys510Glu
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Lys510Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

X-106198312-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198312
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198312
    reference: chr 0
allele count: 2
allele frequency: 2.414554937161208e-5
allele num: 82831
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.760A>G
  hgvsp: ENSP00000440359.1:p.Ser254Gly
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1516A>G
  hgvsp: ENSP00000255495.7:p.Ser506Gly
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1516A>G
  hgvsp: ENSP00000347821.4:p.Ser506Gly
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38148A>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.25e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ser506Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
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X-106198324-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198324
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198324
    reference: chr 0
allele count: 1
allele frequency: 1.254217305690384e-5
allele num: 79731
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.754-6T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1510-6T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1510-6T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38136T>C
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
hgvs: c.1510-6T>C
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS

X-106198347-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198347
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198347
    reference: chr 0
allele count: 1
allele frequency: 1.341453599120006e-5
allele num: 74546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.754-29C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1510-29C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1510-29C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38113C>T
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

X-106198349-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198349
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198349
    reference: chr 0
allele count: 4
allele frequency: 5.405989836739107e-5
allele num: 73992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.754-31G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1510-31G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1510-31G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38111G>A
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

X-106198354-A-ATTCAAACCAAATGCCAAAGGATGAGTCAATCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198354
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198386
    reference: chr 0
allele count: 1
allele frequency: 1.377258704275011e-5
allele num: 72608
alternate allele: ATTCAAACCAAATGCCAAAGGATGAGTCAATCC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
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X-106198361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198361
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198361
    reference: chr 0
allele count: 1
allele frequency: 1.423832101718565e-5
allele num: 70233
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1510-43G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1510-43G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.754-43G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38099G>A
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

X-106198368-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106198368
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106198368
    reference: chr 0
allele count: 1
allele frequency: 1.44971658040853e-5
allele num: 68979
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+38092G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1510-50G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.754-50G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1510-50G>A
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
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site quality: QD

X-106199672-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199672
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199672
    reference: chr 0
allele count: 2
allele frequency: 2.281984870440309e-5
allele num: 87643
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.753+38C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1509+38C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36788C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
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  ensembl gene: ENSG00000133131
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  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1509+38C>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

X-106199673-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199673
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199673
    reference: chr 0
allele count: 4
allele frequency: 4.563917666925288e-5
allele num: 87644
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1509+37A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.753+37A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
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  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1509+37A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36787A>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
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X-106199683-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199683
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199683
    reference: chr 0
allele count: 1
allele frequency: 1.140706097074089e-5
allele num: 87665
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36777T>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1509+27T>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1509+27T>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
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  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.753+27T>A
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1600
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

X-106199691-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199691
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199691
    reference: chr 0
allele count: 1
allele frequency: 1.140406897180914e-5
allele num: 87688
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1509+19C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.753+19C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36769C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1509+19C>T
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2015
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

X-106199692-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199692
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199692
    reference: chr 0
allele count: 1
allele frequency: 1.140315867495296e-5
allele num: 87695
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1509+18C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.753+18C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1509+18C>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36768C>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2015
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

X-106199696-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199696
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199696
    reference: chr 0
allele count: 1
allele frequency: 1.140133851714191e-5
allele num: 87709
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36764C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1509+14C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1509+14C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.753+14C>T
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
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site quality: QD

X-106199716-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199716
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199716
    reference: chr 0
allele count: 1
allele frequency: 1.139847944284233e-5
allele num: 87731
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36744C>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1503C>T
  hgvsp: ENST00000255495.7:c.1503C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1503C>T
  hgvsp: ENST00000355610.4:c.1503C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.747C>T
  hgvsp: ENST00000535534.1:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn501Asn
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

X-106199720-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199720
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199720
    reference: chr 0
allele count: 4
allele frequency: 4.559235872067841e-5
allele num: 87734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36740A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1499A>G
  hgvsp: ENSP00000347821.4:p.Glu500Gly
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.743A>G
  hgvsp: ENSP00000440359.1:p.Glu248Gly
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1499A>G
  hgvsp: ENSP00000255495.7:p.Glu500Gly
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8283
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30285
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4821
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu500Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP

X-106199735-ATCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199735
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199732
    reference: chr 0
allele count: 2
allele frequency: 2.279591953040406e-5
allele num: 87735
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36722_111+36724delAGA
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.725_727delAGA
  hgvsp: ENSP00000440359.1:p.Lys242del
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1481_1483delAGA
  hgvsp: ENSP00000347821.4:p.Lys494del
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1481_1483delAGA
  hgvsp: ENSP00000255495.7:p.Lys494del
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13725
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4819
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
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genotype quality: GenotypeQuality
  all individuals: 44
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3272
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2350
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys494del
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: ATCT
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

X-106199745-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199745
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199742
    reference: chr 0
allele count: 1
allele frequency: 1.139847944284233e-5
allele num: 87731
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1471_1473delGAG
  hgvsp: ENSP00000255495.7:p.Glu491del
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1471_1473delGAG
  hgvsp: ENSP00000347821.4:p.Glu491del
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.715_717delGAG
  hgvsp: ENSP00000440359.1:p.Glu239del
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36712_111+36714delGAG
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10263
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 13701
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1985
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
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  variant carriers: 0
hgvs: p.Glu491del
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: TCTC
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-106199754-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199754
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199754
    reference: chr 0
allele count: 5
allele frequency: 5.700539271015038e-5
allele num: 87711
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1465G>T
  hgvsp: ENSP00000255495.7:p.Val489Phe
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36706G>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1465G>T
  hgvsp: ENSP00000347821.4:p.Val489Phe
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.709G>T
  hgvsp: ENSP00000440359.1:p.Val237Phe
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 6.25e1
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genotype depth: GenotypeDepth
  all individuals: 50
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genotype depth: GenotypeDepth
  all individuals: 3997
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1014
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13653
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genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 15
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4805
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1980
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val489Phe
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-106199776-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199776
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199776
    reference: chr 0
allele count: 3
allele frequency: 3.425556938465579e-5
allele num: 87577
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1455-12A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.699-12A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1455-12A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36684A>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

X-106199792-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199792
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199792
    reference: chr 0
allele count: 1
allele frequency: 1.143680592884019e-5
allele num: 87437
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1455-28A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36668A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1455-28A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.699-28A>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
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X-106199808-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199808
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199808
    reference: chr 0
allele count: 1
allele frequency: 1.146013591721198e-5
allele num: 87259
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.699-44G>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1455-44G>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1455-44G>T
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36652G>T
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
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X-106199811-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106199811
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106199811
    reference: chr 0
allele count: 3
allele frequency: 3.439341480751152e-5
allele num: 87226
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1455-47T>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1455-47T>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36649T>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
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  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.699-47T>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
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site quality: MQRankSum
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site quality: BaseQRankSum
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site quality: DP
site quality: ClippingRankSum

X-106200143-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106200143
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106200143
    reference: chr 0
allele count: 1
allele frequency: 1.156002543205595e-5
allele num: 86505
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1454+23T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1454+23T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36317T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.698+23T>C
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 431
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

X-106200145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106200145
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106200145
    reference: chr 0
allele count: 6
allele frequency: 6.934492164023855e-5
allele num: 86524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36315G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.698+21G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1454+21G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1454+21G>A
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

X-106200149-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106200149
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106200148
    reference: chr 0
allele count: 25
allele frequency: 2.886536041289011e-4
allele num: 86609
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.698+16delG
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36310delG
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1454+16delG
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1454+16delG
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: TC
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

X-106200157-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106200157
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106200157
    reference: chr 0
allele count: 1
allele frequency: 1.153336024450724e-5
allele num: 86705
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.698+9T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1454+9T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1454+9T>C
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36303T>C
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

X-106200158-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106200158
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106200158
    reference: chr 0
allele count: 1
allele frequency: 1.15314982875725e-5
allele num: 86719
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1454+8A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.698+8A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36302A>G
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1454+8A>G
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15169
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3203
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37348
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12088
  bin: 6.25e1
  variant carriers: 0
hgvs: c.1454+8A>G
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-106200162-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106200162
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106200162
    reference: chr 0
allele count: 1
allele frequency: 1.152140100236189e-5
allele num: 86795
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000255495
  ensembl transcript: ENST00000255495
  gene symbol: MORC4
  hgvsc: ENST00000255495.7:c.1454+4G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000474750
  ensembl transcript: ENST00000604604
  gene symbol: MORC4
  hgvsc: ENST00000604604.1:c.111+36298G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000347821
  ensembl transcript: ENST00000355610
  gene symbol: MORC4
  hgvsc: ENST00000355610.4:c.1454+4G>A
  variant of: http://identifiers.org/hgnc/23485
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133131
  ensembl protein: ENSP00000440359
  ensembl transcript: ENST00000535534
  gene symbol: MORC4
  hgvsc: ENST00000535534.1:c.698+4G>A
  variant of: http://identifiers.org/hgnc/23485
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15169
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7719
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12338
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37347
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
hgvs: c.1454+4G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.519433564326605e-4
allele num: 6638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9295
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47988
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.11e-1

QD
type: SiteQuality
SIO_000300: 2.148e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.315e-1

DP
type: SiteQuality
SIO_000300: 1.998458e6

FS
type: SiteQuality
SIO_000300: 5.283e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.004e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.535e0

GenotypeQuality
all individuals: 7292
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2826
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1872
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47988
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9294
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.879470460383324e-5
allele num: 10122
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.87e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.389e0

MQRankSum
type: SiteQuality
SIO_000300: -1.832e0

DP
type: SiteQuality
SIO_000300: 1.997902e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.28e-2

QD
type: SiteQuality
SIO_000300: 2.871e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

GenotypeQuality
all individuals: 2366
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1660
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.167882299003876e-5
allele num: 47986
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.579778830963665e-3
allele num: 633
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 1.086741750642166e-3
allele num: 10122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9294
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.933e1

DP
type: SiteQuality
SIO_000300: 1.998737e6

QD
type: SiteQuality
SIO_000300: 2.789e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.861e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.92e-1

GenotypeQuality
all individuals: 2825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1660
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.083941149501938e-5
allele num: 47986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.879470460383324e-5
allele num: 10122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9294
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

DP
type: SiteQuality
SIO_000300: 1.998737e6

QD
type: SiteQuality
SIO_000300: 2.789e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.861e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

FS
type: SiteQuality
SIO_000300: 5.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.933e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6507
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.08415831266543e-5
allele num: 47981
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9283
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10121
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.481e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.99711e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.585e0

FS
type: SiteQuality
SIO_000300: 9.441000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.407e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.187e1

MQRankSum
type: SiteQuality
SIO_000300: 9.08e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
all individuals: 36966
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6509
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2825
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47978
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.176470588235294e-4
allele num: 8500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10121
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.997049e6

VQSLOD
type: SiteQuality
SIO_000300: -2.881e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 4.179e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.715e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

QD
type: SiteQuality
SIO_000300: 2.361e1

GenotypeQuality
all individuals: 6505
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2367
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9283
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084636230977694e-5
allele num: 47970
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10117
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.29e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.995e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.115e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e0

DP
type: SiteQuality
SIO_000300: 1.996607e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeQuality
all individuals: 1072
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1660
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.077586206896552e-4
allele num: 9280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10112
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8493
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47967
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.324e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.19e-1

DP
type: SiteQuality
SIO_000300: 1.996241e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.547e1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
type: SiteQuality
SIO_000300: -1.32e-1

MQ
type: SiteQuality
SIO_000300: 5.991e1

FS
type: SiteQuality
SIO_000300: 1.083e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10101
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.177717583323519e-4
allele num: 8491
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.08494047494944e-5
allele num: 47963
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

QD
type: SiteQuality
SIO_000300: 2.58e1

FS
type: SiteQuality
SIO_000300: 1.847e0

MQRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.496e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.42e0

DP
type: SiteQuality
SIO_000300: 1.995674e6

VQSLOD
type: SiteQuality
SIO_000300: -3.641e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7281
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variant carriers: 1

GenotypeQuality
all individuals: 1073
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variant carriers: 0

GenotypeQuality
all individuals: 36848
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8487
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.905894006934126e-5
allele num: 10095
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.397e1

MQ
type: SiteQuality
SIO_000300: 5.911e1

DP
type: SiteQuality
SIO_000300: 1.995047e6

VQSLOD
type: SiteQuality
SIO_000300: 2.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

FS
type: SiteQuality
SIO_000300: 4.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10071
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 7.532389273877674e-4
allele num: 6638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9273
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47948
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8451
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.285e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: -6.522e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.21e-1

FS
type: SiteQuality
SIO_000300: 5.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.248e-1

QD
type: SiteQuality
SIO_000300: 1.947e1

DP
type: SiteQuality
SIO_000300: 1.993925e6

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8435
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47940
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9275
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.506931886678722e-4
allele num: 6636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10055
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 1.99248e6

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

FS
type: SiteQuality
SIO_000300: 5.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.504e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9271
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 623
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 5.088540606554041e-4
allele num: 9826
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.367e0

FS
type: SiteQuality
SIO_000300: 1.208e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.14e-2

DP
type: SiteQuality
SIO_000300: 1.980949e6

MQRankSum
type: SiteQuality
SIO_000300: 4.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.39e-1

QD
type: SiteQuality
SIO_000300: 1.319e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1658
bin: 9.25e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9249
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.449479485609308e-4
allele num: 8165
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47605
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.250270855904659e-4
allele num: 9230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.27e-2

FS
type: SiteQuality
SIO_000300: 4.347e0

QD
type: SiteQuality
SIO_000300: 2.044e1

DP
type: SiteQuality
SIO_000300: 1.948465e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.449e0

VQSLOD
type: SiteQuality
SIO_000300: -2.784e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8772
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9227
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.901502186727515e-4
allele num: 47331
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8050
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.926704e6

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.37e-2

QD
type: SiteQuality
SIO_000300: 1.723e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.919999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7987
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.248539564524695e-5
allele num: 47075
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9203
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.661129568106312e-3
allele num: 602
num of homozygotes: 0

South Asian
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allele count: 20
allele frequency: 2.364625206904706e-3
allele num: 8458
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QD
type: SiteQuality
SIO_000300: 2.514e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-2

DP
type: SiteQuality
SIO_000300: 1.912494e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.209e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.013e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

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

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9193
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 602
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6607
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African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 4.250706679985547e-5
allele num: 47051
num of homozygotes: 0

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.909863e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46695
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
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Other
type: Population
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South Asian
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allele frequency: 1.278118609406953e-4
allele num: 7824
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7877
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.889363e6

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.143025523433984e-5
allele num: 46663
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 595
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6593
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.684e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.84e-1

DP
type: SiteQuality
SIO_000300: 1.889109e6

MQRankSum
type: SiteQuality
SIO_000300: -2.921e0

FS
type: SiteQuality
SIO_000300: 7.428e0

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.571e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.4e-1

GenotypeQuality
all individuals: 2682
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1652
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6509
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7729
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4497
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45758
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.202885780372288e-4
allele num: 9079
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6851
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 1.771e1

FS
type: SiteQuality
SIO_000300: 1.665e0

DP
type: SiteQuality
SIO_000300: 1.801137e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

VQSLOD
type: SiteQuality
SIO_000300: -2.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-2

GenotypeQuality
all individuals: 2584
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2289
bin: 8.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 557
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.436622831252072e-3
allele num: 9049
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4487
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45219
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e-1

QD
type: SiteQuality
SIO_000300: 1.798e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-2

DP
type: SiteQuality
SIO_000300: 1.698155e6

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.0e-2

GenotypeQuality
all individuals: 2435
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4190
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2547
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6415
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9021
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44975
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.317349492820445e-4
allele num: 7591
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6181
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4484
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.549e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.874e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

DP
type: SiteQuality
SIO_000300: 1.657951e6

GenotypeQuality
all individuals: 4130
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 5.941770647653001e-4
allele num: 10098
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47959
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 1.860172e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.293e-1

FS
type: SiteQuality
SIO_000300: 5.85e-1

MQ
type: SiteQuality
SIO_000300: 5.992e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.71e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: -5.058e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.63e-1

QD
type: SiteQuality
SIO_000300: 1.885e1

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 8.231420507996237e-4
allele num: 8504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10099
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-2

QD
type: SiteQuality
SIO_000300: 1.694e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.53e-1

FS
type: SiteQuality
SIO_000300: 2.684e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 1.860813e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.691e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeQuality
all individuals: 4118
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2012
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8511
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084723148765844e-5
allele num: 47968
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10105
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-2

MQ
type: SiteQuality
SIO_000300: 5.986e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

DP
type: SiteQuality
SIO_000300: 1.860685e6

QD
type: SiteQuality
SIO_000300: 2.771e1

GenotypeQuality
all individuals: 42200
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6633
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10113
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47974
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.174950064622254e-4
allele num: 8511
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.41e-2

DP
type: SiteQuality
SIO_000300: 1.861802e6

MQ
type: SiteQuality
SIO_000300: 5.989e1

QD
type: SiteQuality
SIO_000300: 1.899e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.69e0

VQSLOD
type: SiteQuality
SIO_000300: 5.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

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

GenotypeQuality
all individuals: 2007
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6635
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.04218776054694e-4
allele num: 47976
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10117
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.555e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.19e-1

QD
type: SiteQuality
SIO_000300: 1.929e1

DP
type: SiteQuality
SIO_000300: 1.86244e6

VQSLOD
type: SiteQuality
SIO_000300: 5.4e0

GenotypeQuality
all individuals: 8201
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42268
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Latino
type: Population
allele count: 24
allele frequency: 2.574002574002574e-3
allele num: 9324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.337328303145257e-5
allele num: 47977
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.579778830963665e-3
allele num: 633
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 8.51e0

QD
type: SiteQuality
SIO_000300: 1.787e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.98e-1

DP
type: SiteQuality
SIO_000300: 1.863397e6

FS
type: SiteQuality
SIO_000300: 5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: 2.33e-1

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2009
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084245190604223e-5
allele num: 47979
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10119
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.320000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.194e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.522e0

MQRankSum
type: SiteQuality
SIO_000300: -6.21e-1

DP
type: SiteQuality
SIO_000300: 1.855869e6

QD
type: SiteQuality
SIO_000300: 3.386e1

MQ
type: SiteQuality
SIO_000300: 5.989e1

GenotypeQuality
all individuals: 1833
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4083
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.875742481398887e-4
allele num: 47981
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.349348055914484e-4
allele num: 8513
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10119
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

QD
type: SiteQuality
SIO_000300: 1.577e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 5.23e-1

DP
type: SiteQuality
SIO_000300: 1.856206e6

VQSLOD
type: SiteQuality
SIO_000300: 8.56e0

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

GenotypeQuality
all individuals: 4075
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2010
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084071441969031e-5
allele num: 47983
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10121
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 3.453e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.16e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

DP
type: SiteQuality
SIO_000300: 1.85365e6

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

GenotypeQuality
all individuals: 565
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42330
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1829
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47985
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.975894092076665e-4
allele num: 10122
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

QD
type: SiteQuality
SIO_000300: 2.032e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.776e-1

FS
type: SiteQuality
SIO_000300: 1.747e0

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

DP
type: SiteQuality
SIO_000300: 1.853829e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

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

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 42336
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10123
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.174674027957242e-4
allele num: 8513
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.006e0

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

FS
type: SiteQuality
SIO_000300: 5.711e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.678e1

VQSLOD
type: SiteQuality
SIO_000300: 7.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.18e-1

DP
type: SiteQuality
SIO_000300: 1.853736e6

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 463
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GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.174674027957242e-4
allele num: 8513
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47983
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10123
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.79e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 1.752e0

DP
type: SiteQuality
SIO_000300: 1.853821e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.192e1

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.87e0

GenotypeQuality
all individuals: 2012
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.083724031589256e-5
allele num: 47991
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.85e-1

FS
type: SiteQuality
SIO_000300: 5.905e0

DP
type: SiteQuality
SIO_000300: 1.853835e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.16e-1

QD
type: SiteQuality
SIO_000300: 1.324e1

VQSLOD
type: SiteQuality
SIO_000300: 6.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.877518767285657e-5
allele num: 10124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47996
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.173999999999999e0

QD
type: SiteQuality
SIO_000300: 1.363e1

DP
type: SiteQuality
SIO_000300: 1.85389e6

FS
type: SiteQuality
SIO_000300: 2.644e0

MQ
type: SiteQuality
SIO_000300: 5.993e1

VQSLOD
type: SiteQuality
SIO_000300: 3.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.161e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 8222
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GenotypeQuality
all individuals: 6
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10125
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.083506958913243e-5
allele num: 47996
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.0e-3

DP
type: SiteQuality
SIO_000300: 1.853594e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.224e-1

QD
type: SiteQuality
SIO_000300: 2.597e1

FS
type: SiteQuality
SIO_000300: 2.236e0

VQSLOD
type: SiteQuality
SIO_000300: -2.449e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.74e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.083593782556153e-5
allele num: 47994
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10125
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.451e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.408e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.58e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 1.853442e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.092e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 4.54e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.083680613435573e-5
allele num: 47992
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.559e1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.853098e6

FS
type: SiteQuality
SIO_000300: 2.625e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.769e0

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.506704836522525e-4
allele num: 6637
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47989
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.492e0

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -7.717000000000001e-1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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African
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allele frequency: 1.174398120963006e-4
allele num: 8515
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 47989
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.197e1

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
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allele num: 10121
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African
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Latino
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Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.083941149501938e-5
allele num: 47986
num of homozygotes: 0

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

Other
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allele num: 632
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47939
num of homozygotes: 0

African
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allele frequency: 1.174536058256989e-4
allele num: 8514
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.656e-1

ReadPosRankSum
type: SiteQuality
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DP
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SIO_000300: 1.846682e6

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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FS
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MQRankSum
type: SiteQuality
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QD
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
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allele frequency: 1.174536058256989e-4
allele num: 8514
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 9309
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

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

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

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.254783863479516e-4
allele num: 47817
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.0329e1

DP
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.62e-1

MQRankSum
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QD
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4511
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9193
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 616
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9138
num of homozygotes: 0

East Asian
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allele frequency: 1.527650473571647e-4
allele num: 6546
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8445
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46958
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.4e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
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QD
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.375e0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.764407e6

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 45637
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 2.405580947798894e-4
allele num: 8314
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8979
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4464
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 602
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East Asian
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.664431e6

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: 1.49e0

MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.59e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8763
num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 1.288992008249549e-4
allele num: 7758
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Other
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InbreedingCoeff
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 4222
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.432143204591886e-5
allele num: 41116
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 8294
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 9.79431929480901e-5
allele num: 40840
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South Asian
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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MQRankSum
type: SiteQuality
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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ReadPosRankSum
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DP
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VQSLOD
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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allele frequency: 1.286504567091213e-4
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European (Non-Finnish)
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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MQ
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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FS
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ReadPosRankSum
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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Latino
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East Asian
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Other
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African
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European (Finnish)
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South Asian
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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DP
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BaseQRankSum
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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East Asian
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Latino
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Other
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DP
type: SiteQuality
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FS
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ClippingRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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Other
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East Asian
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European (Finnish)
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Latino
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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South Asian
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Latino
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East Asian
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African
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European (Non-Finnish)
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DP
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQ
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VQSLOD
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FS
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MQRankSum
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SIO_000300: 3.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.08e0

GenotypeQuality
all individuals: 2351
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4797
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1973
bin: 7.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10063
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.506477854775535e-4
allele num: 6638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47966
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

VQSLOD
type: SiteQuality
SIO_000300: -9.921e-1

FS
type: SiteQuality
SIO_000300: 1.041e0

QD
type: SiteQuality
SIO_000300: 1.297e1

MQRankSum
type: SiteQuality
SIO_000300: -1.387e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.45e-2

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.241e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.134e0

DP
type: SiteQuality
SIO_000300: 3.0754e6

GenotypeQuality
all individuals: 1979
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2351
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10080
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084592774801443e-5
allele num: 47971
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.987e1

DP
type: SiteQuality
SIO_000300: 3.078211e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.112e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.45e-1

FS
type: SiteQuality
SIO_000300: 1.862e0

VQSLOD
type: SiteQuality
SIO_000300: -7.638e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.43e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

QD
type: SiteQuality
SIO_000300: 1.061e1

GenotypeQuality
all individuals: 2351
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4811
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.17426021606388e-4
allele num: 8516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.751e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.46e-2

QD
type: SiteQuality
SIO_000300: 1.385e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.54e0

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

DP
type: SiteQuality
SIO_000300: 3.078397e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
all individuals: 3273
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1977
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.17426021606388e-4
allele num: 8516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

DP
type: SiteQuality
SIO_000300: 3.079469e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.898e0

MQRankSum
type: SiteQuality
SIO_000300: 6.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 2.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.35e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.648e0

QD
type: SiteQuality
SIO_000300: 1.392e1

GenotypeQuality
all individuals: 4821
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2803
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2351
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47980
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.887284951552304e-5
allele num: 10114
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.081303e6

FS
type: SiteQuality
SIO_000300: 1.957e0

MQ
type: SiteQuality
SIO_000300: 5.848e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.517e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-2

QD
type: SiteQuality
SIO_000300: 3.114e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.519e0

MQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

GenotypeQuality
all individuals: 13712
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2351
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2803
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47980
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 6.025911419102139e-4
allele num: 6638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10117
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.73e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.477e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 1.725e1

FS
type: SiteQuality
SIO_000300: 5.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

DP
type: SiteQuality
SIO_000300: 3.081499e6

GenotypeQuality
all individuals: 30284
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2800
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.168229752823976e-5
allele num: 47982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10117
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.02e0

FS
type: SiteQuality
SIO_000300: 3.878e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 5.856e1

QD
type: SiteQuality
SIO_000300: 1.735e1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 3.080696e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

GenotypeQuality
all individuals: 2799
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2351
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4816
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9317
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084114876411988e-5
allele num: 47982
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.84e-1

QD
type: SiteQuality
SIO_000300: 3.399e1

VQSLOD
type: SiteQuality
SIO_000300: -1.469e-1

FS
type: SiteQuality
SIO_000300: 2.464e0

MQ
type: SiteQuality
SIO_000300: 5.841e1

DP
type: SiteQuality
SIO_000300: 3.08021e6

MQRankSum
type: SiteQuality
SIO_000300: -6.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.519999999999999e-2

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.073537305421363e-4
allele num: 9315
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.698144233027954e-4
allele num: 8514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47975
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.67e-2

DP
type: SiteQuality
SIO_000300: 3.079448e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

FS
type: SiteQuality
SIO_000300: 3.219e0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.661e0

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

QD
type: SiteQuality
SIO_000300: 1.448e1

MQ
type: SiteQuality
SIO_000300: 5.989e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9311
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.173622704507513e-5
allele num: 47920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.85e-1

FS
type: SiteQuality
SIO_000300: 2.385e0

DP
type: SiteQuality
SIO_000300: 3.067231e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.218e-1

QD
type: SiteQuality
SIO_000300: 2.935e1

VQSLOD
type: SiteQuality
SIO_000300: -7.356e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30265
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2344
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8509
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.089864158829676e-5
allele num: 47850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9991
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.621e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.401e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.093320215193318e-5
allele num: 47771
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9919
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9295
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6613
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.209e0

FS
type: SiteQuality
SIO_000300: 2.229e0

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.239e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-1

DP
type: SiteQuality
SIO_000300: 2.998461e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.038e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2711
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9294
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9926
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6611
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.527336860670194e-4
allele num: 8505
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47738
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-2

QD
type: SiteQuality
SIO_000300: 2.465e1

MQRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.48e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.991e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.082e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.993261e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

GenotypeQuality
all individuals: 1098
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9290
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8505
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.093714668564968e-5
allele num: 47762
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

FS
type: SiteQuality
SIO_000300: 1.602e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.47e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

DP
type: SiteQuality
SIO_000300: 4.098634e6

GenotypeQuality
all individuals: 1240
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9183
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8503
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47762
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 9.044317154054868e-4
allele num: 6634
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

FS
type: SiteQuality
SIO_000300: 1.208e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.06e-2

DP
type: SiteQuality
SIO_000300: 4.101039e6

QD
type: SiteQuality
SIO_000300: 1.477e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
all individuals: 1570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1267
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9237
num of homozygotes: 0

Latino
type: Population
allele count: 25
allele frequency: 2.688750268875027e-3
allele num: 9298
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47780
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.01e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.43e0

FS
type: SiteQuality
SIO_000300: 5.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.505e-1

QD
type: SiteQuality
SIO_000300: 1.933e1

DP
type: SiteQuality
SIO_000300: 4.104784e6

GenotypeQuality
all individuals: 1056
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.092400401740877e-5
allele num: 47792
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.85e-2

DP
type: SiteQuality
SIO_000300: 4.110351e6

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

MQ
type: SiteQuality
SIO_000300: 5.898e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.732e0

VQSLOD
type: SiteQuality
SIO_000300: -4.326e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.44e-1

QD
type: SiteQuality
SIO_000300: 3.209e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

GenotypeQuality
all individuals: 677
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.092225290819315e-5
allele num: 47796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9331
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

FS
type: SiteQuality
SIO_000300: 2.891e0

QD
type: SiteQuality
SIO_000300: 1.743e1

VQSLOD
type: SiteQuality
SIO_000300: -3.649e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 4.110844e6

MQRankSum
type: SiteQuality
SIO_000300: -5.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3224
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1279
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47809
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9391
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.175917215428034e-4
allele num: 8504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 623
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.9e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.495e0

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3