X-131214002-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214002
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214002
    reference: chr 0
allele count: 1
allele frequency: 1.141122636449739e-5
allele num: 87633
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.1050+32A>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.1005+32A>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.690+32A>T
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  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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  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
  all individuals: 1908
  bin: 9.25e1
  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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  bin: 9.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2303
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 43268
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

X-131214012-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214012
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214012
    reference: chr 0
allele count: 1
allele frequency: 1.140719109326519e-5
allele num: 87664
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.690+22A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.1050+22A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.1005+22A>G
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5411
  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
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genotype depth: GenotypeDepth
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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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
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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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genotype quality: GenotypeQuality
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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: 2429
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

X-131214022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214022
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214022
    reference: chr 0
allele count: 5
allele frequency: 5.701449308414199e-5
allele num: 87697
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.1050+12G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.690+12G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.1005+12G>A
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 6.25e1
  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 depth: GenotypeDepth
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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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genotype quality: GenotypeQuality
  all individuals: 11
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

X-131214028-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214028
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214028
    reference: chr 0
allele count: 1
allele frequency: 1.140120852810398e-5
allele num: 87710
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.1005+6G>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.690+6G>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.1050+6G>C
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 4.25e1
  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
  all individuals: 1908
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 2536
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  variant carriers: 0
hgvs: c.1050+6G>C
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS

X-131214044-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214044
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214044
    reference: chr 0
allele count: 1
allele frequency: 1.139847944284233e-5
allele num: 87731
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.680T>C
  hgvsp: ENSP00000359916.1:p.Val227Ala
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.1040T>C
  hgvsp: ENSP00000298542.3:p.Val347Ala
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.995T>C
  hgvsp: ENSP00000417996.1:p.Val332Ala
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 7.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9586
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 4.75e1
  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
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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: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2435
  bin: 7.75e1
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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
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2536
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val347Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum

X-131214080-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214080
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214080
    reference: chr 0
allele count: 2
allele frequency: 2.279617936033921e-5
allele num: 87734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.959G>A
  hgvsp: ENSP00000417996.1:p.Arg320Gln
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.644G>A
  hgvsp: ENSP00000359916.1:p.Arg215Gln
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.1004G>A
  hgvsp: ENSP00000298542.3:p.Arg335Gln
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 8.25e1
  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
  all individuals: 1908
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 43286
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  variant carriers: 2
hgvs: p.Arg335Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

X-131214081-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214081
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214081
    reference: chr 0
allele count: 1
allele frequency: 1.139847944284233e-5
allele num: 87731
alternate allele: A
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.1003C>T
  hgvsp: ENSP00000298542.3:p.Arg335Ter
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.958C>T
  hgvsp: ENSP00000417996.1:p.Arg320Ter
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.643C>T
  hgvsp: ENSP00000359916.1:p.Arg215Ter
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
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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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 1909
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  variant carriers: 0
genotype depth: GenotypeDepth
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  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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genotype quality: GenotypeQuality
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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: 1568
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg335Ter
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

X-131214086-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214086
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214086
    reference: chr 0
allele count: 2
allele frequency: 2.279643919619755e-5
allele num: 87733
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.638A>T
  hgvsp: ENSP00000359916.1:p.His213Leu
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.953A>T
  hgvsp: ENSP00000417996.1:p.His318Leu
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.998A>T
  hgvsp: ENSP00000298542.3:p.His333Leu
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 2510
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 3924
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43289
  bin: 9.75e1
  variant carriers: 2
hgvs: p.His333Leu
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: T
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

X-131214086-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214086
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214086
    reference: chr 0
allele count: 3
allele frequency: 3.419465879429633e-5
allele num: 87733
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.953A>G
  hgvsp: ENSP00000417996.1:p.His318Arg
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.998A>G
  hgvsp: ENSP00000298542.3:p.His333Arg
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.638A>G
  hgvsp: ENSP00000359916.1:p.His213Arg
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9586
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2411
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2438
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43289
  bin: 9.75e1
  variant carriers: 3
hgvs: p.His333Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

X-131214089-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214089
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214089
    reference: chr 0
allele count: 1
allele frequency: 1.139847944284233e-5
allele num: 87731
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.995A>G
  hgvsp: ENSP00000298542.3:p.Tyr332Cys
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.950A>G
  hgvsp: ENSP00000417996.1:p.Tyr317Cys
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.635A>G
  hgvsp: ENSP00000359916.1:p.Tyr212Cys
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  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
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 1
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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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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  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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1569
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2411
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr332Cys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

X-131214092-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214092
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214092
    reference: chr 0
allele count: 4
allele frequency: 4.559443747862761e-5
allele num: 87730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.632A>G
  hgvsp: ENSP00000359916.1:p.Gln211Arg
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.947A>G
  hgvsp: ENSP00000417996.1:p.Gln316Arg
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.992A>G
  hgvsp: ENSP00000298542.3:p.Gln331Arg
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
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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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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 4
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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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
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1569
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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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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2432
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln331Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

X-131214097-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214097
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214097
    reference: chr 0
allele count: 5
allele frequency: 5.699434616086084e-5
allele num: 87728
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.987A>G
  hgvsp: ENST00000298542.4:c.987A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.627A>G
  hgvsp: ENST00000370879.1:c.627A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.942A>G
  hgvsp: ENST00000464296.1:c.942A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9586
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2438
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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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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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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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: 4434
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43289
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2432
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genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro329Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS

X-131214100-GTAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214100
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214097
    reference: chr 0
allele count: 5
allele frequency: 5.699304684828451e-5
allele num: 87730
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.981_983delTTA
  hgvsp: ENSP00000298542.3:p.Tyr328del
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.936_938delTTA
  hgvsp: ENSP00000417996.1:p.Tyr313del
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.621_623delTTA
  hgvsp: ENSP00000359916.1:p.Tyr208del
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5484
  bin: 3.25e1
  variant carriers: 0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr328del
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: GTAA
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

X-131214101-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214101
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214101
    reference: chr 0
allele count: 1
allele frequency: 1.139964889081416e-5
allele num: 87722
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.983A>G
  hgvsp: ENSP00000298542.3:p.Tyr328Cys
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.623A>G
  hgvsp: ENSP00000359916.1:p.Tyr208Cys
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.938A>G
  hgvsp: ENSP00000417996.1:p.Tyr313Cys
  variant of: http://identifiers.org/hgnc/8079
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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 11
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  variant carriers: 0
hgvs: p.Tyr328Cys
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

X-131214125-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214125
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214125
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87701
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.615-16T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.930-16T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.975-16T>C
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2169
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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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num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

X-131214138-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214138
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214138
    reference: chr 0
allele count: 1
allele frequency: 1.140484934194019e-5
allele num: 87682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.615-29T>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.930-29T>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.975-29T>G
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2342
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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: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: QD

X-131214175-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214175
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214175
    reference: chr 0
allele count: 4
allele frequency: 4.566262171942602e-5
allele num: 87599
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.614+51G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.929+51G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.974+51G>A
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 608
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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
  variant carriers: 4
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

X-131214180-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214180
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214180
    reference: chr 0
allele count: 8
allele frequency: 9.131690390037326e-5
allele num: 87607
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.614+46T>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.974+46T>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.929+46T>G
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

X-131214188-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214188
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214188
    reference: chr 0
allele count: 1
allele frequency: 1.14148735802751e-5
allele num: 87605
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.614+38T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.974+38T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.929+38T>C
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5477
  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
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS

X-131214189-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214189
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214189
    reference: chr 0
allele count: 1
allele frequency: 1.141500388110132e-5
allele num: 87604
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.929+37A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.614+37A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.974+37A>G
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

X-131214192-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214192
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214192
    reference: chr 0
allele count: 1
allele frequency: 1.141409183778293e-5
allele num: 87611
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.974+34T>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.929+34T>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.614+34T>A
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 141
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

X-131214200-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214200
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214200
    reference: chr 0
allele count: 1
allele frequency: 1.14163070529945e-5
allele num: 87594
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.974+26G>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.929+26G>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.614+26G>C
  variant of: http://identifiers.org/hgnc/8079
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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

X-131214200-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214200
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214200
    reference: chr 0
allele count: 4
allele frequency: 4.566522821197799e-5
allele num: 87594
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.974+26G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.929+26G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.614+26G>A
  variant of: http://identifiers.org/hgnc/8079
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 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: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-131214210-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214210
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214210
    reference: chr 0
allele count: 2
allele frequency: 2.283026836980469e-5
allele num: 87603
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.929+16T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.974+16T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.614+16T>C
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 419
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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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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

X-131214213-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214213
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214213
    reference: chr 0
allele count: 1
allele frequency: 1.141643738654915e-5
allele num: 87593
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.974+13G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.614+13G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.929+13G>A
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 4.75e1
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

X-131214222-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214222
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214222
    reference: chr 0
allele count: 1
allele frequency: 1.141565542985651e-5
allele num: 87599
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.929+4C>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.974+4C>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.614+4C>A
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  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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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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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
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genotype quality: GenotypeQuality
  all individuals: 18
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genotype quality: GenotypeQuality
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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: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2601
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28234
  bin: 6.25e1
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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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  bin: 6.75e1
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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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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3411
  bin: 7.75e1
  variant carriers: 0
hgvs: c.974+4C>A
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

X-131214231-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214231
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214231
    reference: chr 0
allele count: 1
allele frequency: 1.141448269564423e-5
allele num: 87608
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.924T>G
  hgvsp: ENSP00000417996.1:p.Phe308Leu
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.969T>G
  hgvsp: ENSP00000298542.3:p.Phe323Leu
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.609T>G
  hgvsp: ENSP00000359916.1:p.Phe203Leu
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.75e1
  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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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.25e1
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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
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
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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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  bin: 6.75e1
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genotype depth: GenotypeDepth
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  bin: 5.75e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 42
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2604
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13202
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Phe323Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-131214236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214236
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214236
    reference: chr 0
allele count: 1
allele frequency: 1.141591607018505e-5
allele num: 87597
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.604C>T
  hgvsp: ENSP00000359916.1:p.Pro202Ser
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.964C>T
  hgvsp: ENSP00000298542.3:p.Pro322Ser
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.919C>T
  hgvsp: ENSP00000417996.1:p.Pro307Ser
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
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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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  bin: 4.75e1
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genotype depth: GenotypeDepth
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  bin: 5.75e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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.Pro322Ser
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS

X-131214237-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214237
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214237
    reference: chr 0
allele count: 1
allele frequency: 1.141565542985651e-5
allele num: 87599
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.963G>T
  hgvsp: ENSP00000298542.3:p.Leu321Phe
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.918G>T
  hgvsp: ENSP00000417996.1:p.Leu306Phe
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.603G>T
  hgvsp: ENSP00000359916.1:p.Leu201Phe
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  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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  bin: 5.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.25e1
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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
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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: 3390
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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
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2605
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu321Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

X-131214246-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214246
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214246
    reference: chr 0
allele count: 39
allele frequency: 4.452969788312667e-4
allele num: 87582
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.594G>T
  hgvsp: ENST00000370879.1:c.594G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.954G>T
  hgvsp: ENST00000298542.4:c.954G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.909G>T
  hgvsp: ENST00000464296.1:c.909G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
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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
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu318Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

X-131214250-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214250
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214250
    reference: chr 0
allele count: 1
allele frequency: 1.142034877745166e-5
allele num: 87563
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.905G>A
  hgvsp: ENSP00000417996.1:p.Arg302Lys
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.950G>A
  hgvsp: ENSP00000298542.3:p.Arg317Lys
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.590G>A
  hgvsp: ENSP00000359916.1:p.Arg197Lys
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 6649
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  variant carriers: 0
hgvs: p.Arg317Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-131214252-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214252
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214252
    reference: chr 0
allele count: 1
allele frequency: 1.142034877745166e-5
allele num: 87563
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.948G>A
  hgvsp: ENST00000298542.4:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.588G>A
  hgvsp: ENST00000370879.1:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.903G>A
  hgvsp: ENST00000464296.1:c.903G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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hgvs: p.Gly316Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP

X-131214263-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214263
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214263
    reference: chr 0
allele count: 8
allele frequency: 9.139827942738978e-5
allele num: 87529
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.937G>A
  hgvsp: ENSP00000298542.3:p.Gly313Arg
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.577G>A
  hgvsp: ENSP00000359916.1:p.Gly193Arg
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.892G>A
  hgvsp: ENSP00000417996.1:p.Gly298Arg
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
hgvs: p.Gly313Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

X-131214265-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214265
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214265
    reference: chr 0
allele count: 1
allele frequency: 1.142569868147437e-5
allele num: 87522
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.935A>G
  hgvsp: ENSP00000298542.3:p.Tyr312Cys
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.575A>G
  hgvsp: ENSP00000359916.1:p.Tyr192Cys
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.890A>G
  hgvsp: ENSP00000417996.1:p.Tyr297Cys
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 4.75e1
  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
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  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: 2.25e1
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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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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13164
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Tyr312Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

X-131214297-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214297
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214297
    reference: chr 0
allele count: 2
allele frequency: 2.304412950800784e-5
allele num: 86790
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.906-3T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.861-3T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.546-3T>C
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.75e1
  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 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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 26397
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  variant carriers: 0
hgvs: c.906-3T>C
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

X-131214298-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214298
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214298
    reference: chr 0
allele count: 1
allele frequency: 1.152246304169979e-5
allele num: 86787
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.906-4A>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.861-4A>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.546-4A>T
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
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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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 2269
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  variant carriers: 0
hgvs: c.906-4A>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD

X-131214300-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214300
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214300
    reference: chr 0
allele count: 1
allele frequency: 1.155601779626741e-5
allele num: 86535
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.861-6T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.906-6T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.546-6T>C
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
  all individuals: 1209
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  variant carriers: 0
hgvs: c.906-6T>C
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

X-131214304-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214304
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214304
    reference: chr 0
allele count: 2
allele frequency: 2.311737848927932e-5
allele num: 86515
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.546-10C>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.861-10C>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.906-10C>T
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  bin: 9.25e1
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num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD

X-131214314-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214314
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214314
    reference: chr 0
allele count: 2
allele frequency: 2.322394853573004e-5
allele num: 86118
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.906-20T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.546-20T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.861-20T>C
  variant of: http://identifiers.org/hgnc/8079
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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num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

X-131214317-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214317
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214317
    reference: chr 0
allele count: 1
allele frequency: 1.163155874518744e-5
allele num: 85973
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.546-23A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.861-23A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
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  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.906-23A>G
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
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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: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

X-131214323-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214323
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214323
    reference: chr 0
allele count: 1
allele frequency: 1.166534459427932e-5
allele num: 85724
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.906-29C>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.546-29C>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
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  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.861-29C>A
  variant of: http://identifiers.org/hgnc/8079
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 quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

X-131214324-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214324
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214324
    reference: chr 0
allele count: 2
allele frequency: 2.333640596011808e-5
allele num: 85703
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.546-30A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.861-30A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.906-30A>G
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

X-131214326-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214326
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214326
    reference: chr 0
allele count: 19
allele frequency: 2.231644722160232e-4
allele num: 85139
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.861-32G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.546-32G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.906-32G>A
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
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X-131214340-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214340
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214340
    reference: chr 0
allele count: 1
allele frequency: 1.182144883676944e-5
allele num: 84592
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.546-46T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.861-46T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.906-46T>C
  variant of: http://identifiers.org/hgnc/8079
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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
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X-131214341-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131214341
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131214341
    reference: chr 0
allele count: 1
allele frequency: 1.182536303864529e-5
allele num: 84564
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.906-47A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.546-47A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.861-47A>G
  variant of: http://identifiers.org/hgnc/8079
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 quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

X-131216356-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216356
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216356
    reference: chr 0
allele count: 1
allele frequency: 1.139588152841563e-5
allele num: 87751
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.545+35A>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.860+35A>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.905+35A>C
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1417
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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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  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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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: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-131216359-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216359
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216359
    reference: chr 0
allele count: 7
allele frequency: 7.977298886596998e-5
allele num: 87749
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.860+32C>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.545+32C>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.905+32C>G
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
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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 depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 7
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 10868
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  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-131216372-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216372
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216372
    reference: chr 0
allele count: 1
allele frequency: 1.139575166377974e-5
allele num: 87752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.545+19T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.905+19T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.860+19T>C
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1106
  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 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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  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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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

X-131216373-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216373
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216373
    reference: chr 0
allele count: 1
allele frequency: 1.139575166377974e-5
allele num: 87752
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.860+18A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.545+18A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.905+18A>G
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

X-131216376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216376
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216376
    reference: chr 0
allele count: 1
allele frequency: 1.139575166377974e-5
allele num: 87752
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.905+15C>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.860+15C>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.545+15C>T
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 6.25e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2713
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 6264
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

X-131216379-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216379
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216379
    reference: chr 0
allele count: 1
allele frequency: 1.139575166377974e-5
allele num: 87752
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.860+12A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.545+12A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.905+12A>G
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-131216382-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216382
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216382
    reference: chr 0
allele count: 1
allele frequency: 1.13954919433872e-5
allele num: 87754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.545+9A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.860+9A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.905+9A>G
  variant of: http://identifiers.org/hgnc/8079
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 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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  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-131216397-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216397
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216397
    reference: chr 0
allele count: 3
allele frequency: 3.418647583016159e-5
allele num: 87754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.854G>A
  hgvsp: ENSP00000417996.1:p.Arg285His
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.539G>A
  hgvsp: ENSP00000359916.1:p.Arg180His
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.899G>A
  hgvsp: ENSP00000298542.3:p.Arg300His
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7524
  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
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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hgvs: p.Arg300His
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP

X-131216398-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216398
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216398
    reference: chr 0
allele count: 26
allele frequency: 2.962794142783887e-4
allele num: 87755
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.853C>T
  hgvsp: ENSP00000417996.1:p.Arg285Cys
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.898C>T
  hgvsp: ENSP00000298542.3:p.Arg300Cys
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.538C>T
  hgvsp: ENSP00000359916.1:p.Arg180Cys
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7524
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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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hgvs: p.Arg300Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

X-131216404-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216404
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216404
    reference: chr 0
allele count: 4
allele frequency: 4.558092893933178e-5
allele num: 87756
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.892A>G
  hgvsp: ENSP00000298542.3:p.Ser298Gly
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.847A>G
  hgvsp: ENSP00000417996.1:p.Ser283Gly
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.532A>G
  hgvsp: ENSP00000359916.1:p.Ser178Gly
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7526
  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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  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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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1109
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genotype depth: GenotypeDepth
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  bin: 8.25e1
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genotype depth: GenotypeDepth
  all individuals: 7428
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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: 4
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
  all individuals: 6
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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genotype quality: GenotypeQuality
  all individuals: 13
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 4
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3175
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2489
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10917
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser298Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

X-131216421-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216421
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216421
    reference: chr 0
allele count: 3
allele frequency: 3.418491761434855e-5
allele num: 87758
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.875T>C
  hgvsp: ENSP00000298542.3:p.Leu292Pro
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.830T>C
  hgvsp: ENSP00000417996.1:p.Leu277Pro
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.515T>C
  hgvsp: ENSP00000359916.1:p.Leu172Pro
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
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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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genotype depth: GenotypeDepth
  all individuals: 5713
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  variant carriers: 3
genotype depth: GenotypeDepth
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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: 6
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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: 29850
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  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu292Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

X-131216423-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216423
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216423
    reference: chr 0
allele count: 1
allele frequency: 1.139484269419661e-5
allele num: 87759
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.513A>G
  hgvsp: ENST00000370879.1:c.513A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.873A>G
  hgvsp: ENST00000298542.4:c.873A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.828A>G
  hgvsp: ENST00000464296.1:c.828A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4012
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 1
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  variant carriers: 0
hgvs: p.Leu291Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

X-131216426-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216426
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216426
    reference: chr 0
allele count: 2
allele frequency: 2.279020476998986e-5
allele num: 87757
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.510C>T
  hgvsp: ENST00000370879.1:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.870C>T
  hgvsp: ENST00000298542.4:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.825C>T
  hgvsp: ENST00000464296.1:c.825C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5298
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 1569
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  variant carriers: 0
hgvs: p.Thr290Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

X-131216426-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216426
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216426
    reference: chr 0
allele count: 4
allele frequency: 4.558040953997972e-5
allele num: 87757
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.870C>G
  hgvsp: ENST00000298542.4:c.870C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.510C>G
  hgvsp: ENST00000370879.1:c.510C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.825C>G
  hgvsp: ENST00000464296.1:c.825C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 8.75e1
  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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  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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  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
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  bin: 7.75e1
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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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: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr290Thr
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-131216444-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216444
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216444
    reference: chr 0
allele count: 1
allele frequency: 1.139562180210363e-5
allele num: 87753
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.492C>T
  hgvsp: ENST00000370879.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.807C>T
  hgvsp: ENST00000464296.1:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.852C>T
  hgvsp: ENST00000298542.4:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10902
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genotype quality: GenotypeQuality
  all individuals: 29844
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro284Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

X-131216453-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216453
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216453
    reference: chr 0
allele count: 17
allele frequency: 1.937321937321937e-4
allele num: 87750
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.843G>A
  hgvsp: ENST00000298542.4:c.843G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.483G>A
  hgvsp: ENST00000370879.1:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.798G>A
  hgvsp: ENST00000464296.1:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7528
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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 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: 2
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genotype quality: GenotypeQuality
  all individuals: 2713
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  variant carriers: 0
hgvs: p.Ser281Ser
num of homozygotes: 1
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-131216454-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216454
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216454
    reference: chr 0
allele count: 4223
allele frequency: 4.812974402224704e-2
allele num: 87742
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.842C>T
  hgvsp: ENSP00000298542.3:p.Ser281Leu
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.797C>T
  hgvsp: ENSP00000417996.1:p.Ser266Leu
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.482C>T
  hgvsp: ENSP00000359916.1:p.Ser161Leu
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 28
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 2689
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser281Leu
num of homozygotes: 105
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

X-131216517-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216517
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216517
    reference: chr 0
allele count: 1
allele frequency: 1.140016872249709e-5
allele num: 87718
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.734G>C
  hgvsp: ENSP00000417996.1:p.Ser245Thr
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.779G>C
  hgvsp: ENSP00000298542.3:p.Ser260Thr
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.419G>C
  hgvsp: ENSP00000359916.1:p.Ser140Thr
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2615
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3878
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3340
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2839
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11544
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6553
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser260Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

X-131216518-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216518
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216518
    reference: chr 0
allele count: 16
allele frequency: 1.824006201621086e-4
allele num: 87719
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.778A>G
  hgvsp: ENSP00000298542.3:p.Ser260Gly
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.418A>G
  hgvsp: ENSP00000359916.1:p.Ser140Gly
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.733A>G
  hgvsp: ENSP00000417996.1:p.Ser245Gly
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7832
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 3879
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28113
  bin: 9.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 2616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6552
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2839
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11535
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser260Gly
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

X-131216541-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216541
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216540
    reference: chr 0
allele count: 1
allele frequency: 1.14047192728351e-5
allele num: 87683
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.394delG
  hgvsp: ENSP00000359916.1:p.Asp132IlefsTer67
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.754delG
  hgvsp: ENSP00000298542.3:p.Asp252IlefsTer67
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.709delG
  hgvsp: ENSP00000417996.1:p.Asp237IlefsTer67
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7804
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10801
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2841
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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: 2600
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genotype quality: GenotypeQuality
  all individuals: 2
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3879
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1667
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genotype quality: GenotypeQuality
  all individuals: 9
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 34
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6535
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3337
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp252IlefsTer67
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: TC
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP

X-131216543-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216543
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216543
    reference: chr 0
allele count: 1
allele frequency: 1.140445914352512e-5
allele num: 87685
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.393G>T
  hgvsp: ENSP00000359916.1:p.Lys131Asn
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.753G>T
  hgvsp: ENSP00000298542.3:p.Lys251Asn
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.708G>T
  hgvsp: ENSP00000417996.1:p.Lys236Asn
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2596
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3878
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2841
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 28101
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
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genotype quality: GenotypeQuality
  all individuals: 13
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genotype quality: GenotypeQuality
  all individuals: 6532
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genotype quality: GenotypeQuality
  all individuals: 3
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3337
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11510
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys251Asn
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

X-131216544-TTGC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216544
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216541
    reference: chr 0
allele count: 1
allele frequency: 1.140523956705711e-5
allele num: 87679
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  consequence: stop_gained
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.749_751delGCA
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: stop_gained
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.389_391delGCA
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: stop_gained
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.704_706delGCA
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 7869
  bin: 3.75e1
  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 depth: GenotypeDepth
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  variant carriers: 0
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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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.75e1
  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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genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 8.25e1
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genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
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genotype depth: GenotypeDepth
  all individuals: 891
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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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
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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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: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28101
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Cys250_Lys251delinsTer
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: TTGC
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

X-131216583-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216583
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216583
    reference: chr 0
allele count: 8
allele frequency: 9.146724900815201e-5
allele num: 87463
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.697-29T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.742-29T>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.382-29T>C
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10262
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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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genotype quality: GenotypeQuality
  all individuals: 277
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-131216596-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216596
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216596
    reference: chr 0
allele count: 1
allele frequency: 1.145081873353945e-5
allele num: 87330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.382-42T>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.742-42T>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.697-42T>A
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
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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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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 3733
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

X-131216600-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216600
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216600
    reference: chr 0
allele count: 53
allele frequency: 6.080770995869665e-4
allele num: 87160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.382-46G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.697-46G>A
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.742-46G>A
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1197
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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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: 5
genotype quality: GenotypeQuality
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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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 5763
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

X-131216605-A-ATTGCAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131216605
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131216611
    reference: chr 0
allele count: 1
allele frequency: 1.147776183644189e-5
allele num: 87125
alternate allele: ATTGCAC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.697-52_697-51insGTGCAA
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.382-52_382-51insGTGCAA
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.742-52_742-51insGTGCAA
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2483
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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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: 4.75e1
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num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

X-131218472-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131218472
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131218472
    reference: chr 0
allele count: 1
allele frequency: 1.145750982481467e-5
allele num: 87279
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.741+46A>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.381+46A>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.696+46A>T
  variant of: http://identifiers.org/hgnc/8079
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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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: 3424
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  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

X-131218475-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131218475
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131218475
    reference: chr 0
allele count: 1
allele frequency: 1.145803494700659e-5
allele num: 87275
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.381+43G>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.696+43G>C
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.741+43G>C
  variant of: http://identifiers.org/hgnc/8079
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 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: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

X-131218478-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131218478
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131218478
    reference: chr 0
allele count: 1
allele frequency: 1.145619722989151e-5
allele num: 87289
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.696+40C>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.741+40C>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.381+40C>T
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4717
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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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num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
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X-131218479-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131218479
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131218479
    reference: chr 0
allele count: 1
allele frequency: 1.145540981728621e-5
allele num: 87295
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.696+39A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.741+39A>G
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.381+39A>G
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.25e1
  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
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8676
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2500
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3402
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31652
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7493
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
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: T
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

X-131218485-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131218485
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131218485
    reference: chr 0
allele count: 38
allele frequency: 4.351759599638117e-4
allele num: 87321
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.741+33C>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.381+33C>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.696+33C>T
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8680
  bin: 9.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3399
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32076
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2431
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2505
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

X-131218495-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24131218495
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24131218495
    reference: chr 0
allele count: 6
allele frequency: 6.867581581146199e-5
allele num: 87367
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000417996
  ensembl transcript: ENST00000464296
  gene symbol: FRMD7
  hgvsc: ENST00000464296.1:c.696+23C>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000359916
  ensembl transcript: ENST00000370879
  gene symbol: FRMD7
  hgvsc: ENST00000370879.1:c.381+23C>T
  variant of: http://identifiers.org/hgnc/8079
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165694
  ensembl protein: ENSP00000298542
  ensembl transcript: ENST00000298542
  gene symbol: FRMD7
  hgvsc: ENST00000298542.4:c.741+23C>T
  variant of: http://identifiers.org/hgnc/8079
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 4.75e1
  variant carriers: 2
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 1451
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8475
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6621
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.085244807740429e-5
allele num: 47956
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10110
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -7.679e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

MQRankSum
type: SiteQuality
SIO_000300: 5.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.44e-2

FS
type: SiteQuality
SIO_000300: 2.868e0

DP
type: SiteQuality
SIO_000300: 3.774425e6

QD
type: SiteQuality
SIO_000300: 2.52e1

GenotypeQuality
all individuals: 80
bin: 2.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
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: 47966
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.11e0

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

DP
type: SiteQuality
SIO_000300: 3.77714e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

QD
type: SiteQuality
SIO_000300: 1.565e1

VQSLOD
type: SiteQuality
SIO_000300: 6.889999999999999e-1

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10119
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: 6623
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 5.365958360163126e-4
allele num: 9318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47971
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.931e0

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-1

DP
type: SiteQuality
SIO_000300: 3.778516e6

VQSLOD
type: SiteQuality
SIO_000300: -1.354e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.97e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.27e-1

FS
type: SiteQuality
SIO_000300: 5.675e0

QD
type: SiteQuality
SIO_000300: 1.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e-1

GenotypeQuality
all individuals: 43283
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
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: 10118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084288632289799e-5
allele num: 47978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

VQSLOD
type: SiteQuality
SIO_000300: -6.774e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.398e0

DP
type: SiteQuality
SIO_000300: 3.778806e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.276e1

FS
type: SiteQuality
SIO_000300: 3.886e0

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.508750754375377e-4
allele num: 6628
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: 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: 47987
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.771e1

VQSLOD
type: SiteQuality
SIO_000300: -2.193e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.92e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.620000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

FS
type: SiteQuality
SIO_000300: 4.659e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

DP
type: SiteQuality
SIO_000300: 3.77933e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

GenotypeQuality
all individuals: 1471
bin: 7.25e1
variant carriers: 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: 1.174536058256989e-4
allele num: 8514
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.508750754375377e-4
allele num: 6628
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 4.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.304e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.370000000000001e-2

DP
type: SiteQuality
SIO_000300: 3.779716e6

GenotypeQuality
all individuals: 2434
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1472
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9318
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: 6626
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: 8514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.08385429690756e-5
allele num: 47988
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.779684e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.91e-1

FS
type: SiteQuality
SIO_000300: 7.284e0

VQSLOD
type: SiteQuality
SIO_000300: -2.555e-1

QD
type: SiteQuality
SIO_000300: 1.688e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.633e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.23e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.63e-1

MQ
type: SiteQuality
SIO_000300: 5.991e1

GenotypeQuality
all individuals: 2438
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.017046311660884e-4
allele num: 6629
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47987
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: 10123
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

DP
type: SiteQuality
SIO_000300: 3.779707e6

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 8.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.907e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

QD
type: SiteQuality
SIO_000300: 2.166e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

African
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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: 2.963548355230663e-4
allele num: 10123
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 47987
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.907e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

FS
type: SiteQuality
SIO_000300: 8.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.083984578514119e-5
allele num: 47985
num of homozygotes: 0

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

South Asian
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East 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: 633
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.991e1

DP
type: SiteQuality
SIO_000300: 3.779764e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

African
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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
allele num: 6628
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 8.335938314056477e-5
allele num: 47985
num of homozygotes: 0

Latino
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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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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.034e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 3.779839e6

ReadPosRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.11e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

Latino
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allele frequency: 1.073191672032625e-4
allele num: 9318
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 6627
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47984
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

BaseQRankSum
type: SiteQuality
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DP
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.725e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 1

South Asian
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allele frequency: 0.0e0
allele num: 10122
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

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

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

East Asian
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allele count: 5
allele frequency: 7.54261577915221e-4
allele num: 6629
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.181e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.57e-1

DP
type: SiteQuality
SIO_000300: 3.779784e6

MQ
type: SiteQuality
SIO_000300: 5.656e1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

QD
type: SiteQuality
SIO_000300: 2.054e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6621
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.083984578514119e-5
allele num: 47985
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e0

DP
type: SiteQuality
SIO_000300: 3.779203e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

QD
type: SiteQuality
SIO_000300: 8.800000000000001e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6615
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.44e-1

DP
type: SiteQuality
SIO_000300: 3.77815e6

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.1946e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.721e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.712e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
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allele frequency: 9.880446596186147e-5
allele num: 10121
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 count: 0
allele frequency: 0.0e0
allele num: 9314
num of homozygotes: 0

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

East Asian
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Other
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allele count: 0
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allele num: 631
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.91e-2

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.872e1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47941
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 4.300612837329319e-4
allele num: 9301
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

South Asian
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 8511
num of homozygotes: 0

VQSLOD
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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DP
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47946
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 6579
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 8.224650452355775e-4
allele num: 8511
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele num: 9300
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South Asian
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
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num of homozygotes: 0

Latino
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African
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allele frequency: 0.0e0
allele num: 8511
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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DP
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

Other
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num of homozygotes: 0

South Asian
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European (Finnish)
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Latino
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African
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East Asian
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European (Non-Finnish)
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FS
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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QD
type: SiteQuality
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BaseQRankSum
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DP
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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East Asian
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Latino
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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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ClippingRankSum
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QD
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InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

Latino
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European (Non-Finnish)
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European (Finnish)
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allele num: 4523
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African
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Other
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South Asian
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East Asian
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VQSLOD
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FS
type: SiteQuality
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DP
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MQ
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QD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Other
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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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East Asian
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allele frequency: 3.044140030441401e-4
allele num: 6570
num of homozygotes: 0

South Asian
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allele frequency: 9.885330170027679e-5
allele num: 10116
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 4523
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European (Non-Finnish)
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allele frequency: 2.085679723021733e-5
allele num: 47946
num of homozygotes: 0

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
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FS
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 9298
num of homozygotes: 0

African
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allele frequency: 2.349624060150376e-4
allele num: 8512
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 10116
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European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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VQSLOD
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MQ
type: SiteQuality
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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FS
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DP
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ClippingRankSum
type: SiteQuality
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QD
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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African
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allele frequency: 0.0e0
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Other
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East Asian
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allele frequency: 1.522765341860819e-4
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 10115
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 47947
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 47949
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African
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allele num: 8512
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Latino
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allele frequency: 0.0e0
allele num: 9303
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East Asian
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allele frequency: 1.522765341860819e-4
allele num: 6567
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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InbreedingCoeff
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QD
type: SiteQuality
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MQ
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FS
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BaseQRankSum
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.76e-1

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

African
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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
allele num: 10112
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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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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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.085462242706096e-5
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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DP
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 630
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4524
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South Asian
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allele frequency: 9.890218573830482e-5
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DP
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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African
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allele frequency: 1.174812030075188e-4
allele num: 8512
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South Asian
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Latino
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East Asian
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allele count: 0
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Other
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allele count: 0
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e-1

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

South Asian
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allele num: 10109
num of homozygotes: 0

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

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

Other
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East Asian
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Latino
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allele frequency: 4.300612837329319e-4
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African
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allele frequency: 4.112325226177887e-3
allele num: 8511
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
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QD
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Finnish)
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African
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Other
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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MQ
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MQRankSum
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ClippingRankSum
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FS
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DP
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VQSLOD
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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European (Finnish)
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Latino
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Other
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South Asian
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European (Non-Finnish)
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East Asian
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African
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QD
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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GenotypeQuality
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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Other
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East Asian
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Latino
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VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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QD
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GenotypeQuality
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variant carriers: 0

South Asian
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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African
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Other
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BaseQRankSum
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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ClippingRankSum
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DP
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
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South Asian
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Latino
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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MQ
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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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ClippingRankSum
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DP
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ReadPosRankSum
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MQRankSum
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QD
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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African
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Latino
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MQ
type: SiteQuality
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VQSLOD
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SIO_000300: 1.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.09e-2

DP
type: SiteQuality
SIO_000300: 2.277286e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.672e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4492
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6453
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47304
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8455
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.079913606911447e-4
allele num: 9260
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e0

VQSLOD
type: SiteQuality
SIO_000300: -6.977e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

DP
type: SiteQuality
SIO_000300: 2.255634e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-1

FS
type: SiteQuality
SIO_000300: 6.292e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.551e1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47293
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 8452
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East Asian
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allele frequency: 1.550387596899225e-4
allele num: 6450
num of homozygotes: 0

South Asian
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allele frequency: 1.005429318318922e-4
allele num: 9946
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4491
num of homozygotes: 0

MQ
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 2.253425e6

VQSLOD
type: SiteQuality
SIO_000300: 5.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.17e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4486
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6393
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 2.167551750298038e-4
allele num: 9227
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9892
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47060
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.658e0

DP
type: SiteQuality
SIO_000300: 2.200562e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

QD
type: SiteQuality
SIO_000300: 1.478e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8423
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46966
num of homozygotes: 0

South Asian
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allele frequency: 1.012555690562981e-4
allele num: 9876
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4480
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.174415e6

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

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.528e0

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.028e0

QD
type: SiteQuality
SIO_000300: 1.938e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9854
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46824
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African
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allele count: 1
allele frequency: 1.189909566872918e-4
allele num: 8404
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 621
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4474
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East Asian
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allele num: 6345
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MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.931e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.3134e1

MQ
type: SiteQuality
SIO_000300: 5.882e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.88e-1

QD
type: SiteQuality
SIO_000300: 1.54e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.136706480630756e-5
allele num: 46801
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.576541068894845e-4
allele num: 6343
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8409
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4475
num of homozygotes: 0

Latino
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allele count: 0
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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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 622
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-2

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.92e-1

DP
type: SiteQuality
SIO_000300: 2.126868e6

QD
type: SiteQuality
SIO_000300: 1.394e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 9841
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6325
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African
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allele count: 4
allele frequency: 4.805382027871216e-4
allele num: 8324
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele count: 1
allele frequency: 1.088968746596973e-4
allele num: 9183
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European (Non-Finnish)
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allele count: 14
allele frequency: 3.0139286560031e-4
allele num: 46451
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 612
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FS
type: SiteQuality
SIO_000300: 3.0446e1

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.905e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

QD
type: SiteQuality
SIO_000300: 5.3e-1

DP
type: SiteQuality
SIO_000300: 2.11574e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.27e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4451
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.168962151610454e-5
allele num: 46105
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Latino
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allele count: 0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 616
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.032385e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.456e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46097
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4451
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Other
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South Asian
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East Asian
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African
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Latino
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allele num: 9142
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 8.64e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.032024e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
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num of homozygotes: 0

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

Latino
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Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.083420142505938e-5
allele num: 47998
num of homozygotes: 0

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

GenotypeQuality
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bin: 9.25e1
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African
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.250078129883118e-4
allele num: 47997
num of homozygotes: 0

Latino
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allele frequency: 1.072731173567904e-4
allele num: 9322
num of homozygotes: 0

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

East Asian
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South Asian
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.743293e6

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

African
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num of homozygotes: 0

Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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allele frequency: 9.877518767285657e-5
allele num: 10124
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Other
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allele num: 633
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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DP
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
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VQSLOD
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GenotypeQuality
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Latino
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num of homozygotes: 0

Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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African
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ClippingRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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FS
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QD
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MQRankSum
type: SiteQuality
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VQSLOD
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DP
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GenotypeQuality
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South Asian
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African
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East Asian
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Latino
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num of homozygotes: 0

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

BaseQRankSum
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DP
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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GenotypeQuality
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Other
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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QD
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FS
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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East Asian
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African
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allele frequency: 1.174812030075188e-4
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Latino
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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FS
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

East Asian
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African
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 6.250260427517813e-5
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European (Finnish)
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Other
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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ReadPosRankSum
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QD
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VQSLOD
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FS
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DP
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GenotypeQuality
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bin: 6.75e1
variant carriers: 1

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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allele num: 9322
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European (Finnish)
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East Asian
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African
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allele frequency: 2.93703007518797e-3
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Other
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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DP
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 8.333680570023751e-5
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East Asian
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Latino
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Other
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South Asian
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ClippingRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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MQRankSum
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QD
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DP
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VQSLOD
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FS
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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East Asian
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Latino
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African
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South Asian
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MQ
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BaseQRankSum
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FS
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VQSLOD
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QD
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ClippingRankSum
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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DP
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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South Asian
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FS
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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DP
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MQ
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QD
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

Latino
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Other
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South Asian
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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QD
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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MQ
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MQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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East Asian
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European (Finnish)
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South Asian
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Latino
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Other
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African
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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FS
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DP
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QD
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InbreedingCoeff
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MQ
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GenotypeQuality
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variant carriers: 0

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