11-72468902-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468902
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468902
    reference: chr 11
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.83C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.487C>T
  hgvsp: ENSP00000445657.1:p.Arg163Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.349C>T
  hgvsp: ENSP00000440016.1:p.Arg117Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.487C>T
  hgvsp: ENSP00000438792.1:p.Arg163Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.487C>T
  hgvsp: ENSP00000443597.1:p.Arg163Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.208C>T
  hgvsp: ENSP00000445708.1:p.Arg70Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.280C>T
  hgvsp: ENSP00000438357.1:p.Arg94Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.400C>T
  hgvsp: ENSP00000443548.1:p.Arg134Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.280C>T
  hgvsp: ENSP00000442414.1:p.Arg94Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.487C>T
  hgvsp: ENSP00000335247.6:p.Arg163Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+673C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000444027
  ensembl transcript: ENST00000400925
  gene symbol: STARD10
  hgvsc: ENST00000400925.2:c.26C>T
  hgvsp: ENSP00000444027.1:p.Arg10Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25260C>T
  variant of: http://identifiers.org/hgnc/16925
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg163Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-72468902-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468902
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468902
    reference: chr 11
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.280C>A
  hgvsp: ENST00000536728.1:c.280C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.349C>A
  hgvsp: ENST00000538536.1:c.349C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.487C>A
  hgvsp: ENST00000537947.1:c.487C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000444027
  ensembl transcript: ENST00000400925
  gene symbol: STARD10
  hgvsc: ENST00000400925.2:c.26C>A
  hgvsp: ENST00000400925.2:c.26C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.487C>A
  hgvsp: ENST00000543304.1:c.487C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.208C>A
  hgvsp: ENST00000537351.1:c.208C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.83C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+673C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.487C>A
  hgvsp: ENST00000542989.1:c.487C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.400C>A
  hgvsp: ENST00000545082.1:c.400C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.487C>A
  hgvsp: ENST00000334805.6:c.487C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25260C>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.280C>A
  hgvsp: ENST00000544767.1:c.280C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg163Arg
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

11-72468916-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468916
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468916
    reference: chr 11
allele count: 1
allele frequency: 8.296689620841284e-6
allele num: 120530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000444027
  ensembl transcript: ENST00000400925
  gene symbol: STARD10
  hgvsc: ENST00000400925.2:c.12G>A
  hgvsp: ENSP00000444027.1:p.Arg5Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.473G>A
  hgvsp: ENSP00000445657.1:p.Arg158Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+659G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.473G>A
  hgvsp: ENSP00000443597.1:p.Arg158Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.266G>A
  hgvsp: ENSP00000442414.1:p.Arg89Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.335G>A
  hgvsp: ENSP00000440016.1:p.Arg112Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.194G>A
  hgvsp: ENSP00000445708.1:p.Arg65Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.69G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.386G>A
  hgvsp: ENSP00000443548.1:p.Arg129Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.266G>A
  hgvsp: ENSP00000438357.1:p.Arg89Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.473G>A
  hgvsp: ENSP00000438792.1:p.Arg158Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25274G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.473G>A
  hgvsp: ENSP00000335247.6:p.Arg158Gln
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9326
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg158Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

11-72468922-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468922
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468922
    reference: chr 11
allele count: 1
allele frequency: 8.295726041943191e-6
allele num: 120544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.63C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.260C>A
  hgvsp: ENSP00000442414.1:p.Pro87Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.260C>A
  hgvsp: ENSP00000438357.1:p.Pro87Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.467C>A
  hgvsp: ENSP00000443597.1:p.Pro156Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.329C>A
  hgvsp: ENSP00000440016.1:p.Pro110Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.188C>A
  hgvsp: ENSP00000445708.1:p.Pro63Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.380C>A
  hgvsp: ENSP00000443548.1:p.Pro127Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+653C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.467C>A
  hgvsp: ENSP00000438792.1:p.Pro156Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.467C>A
  hgvsp: ENSP00000445657.1:p.Pro156Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.467C>A
  hgvsp: ENSP00000335247.6:p.Pro156Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000444027
  ensembl transcript: ENST00000400925
  gene symbol: STARD10
  hgvsc: ENST00000400925.2:c.6C>A
  hgvsp: ENSP00000444027.1:p.Pro3Gln
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25280C>A
  variant of: http://identifiers.org/hgnc/16925
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro156Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

11-72468924-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468924
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468924
    reference: chr 11
allele count: 8
allele frequency: 6.636690945894378e-5
allele num: 120542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.61C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25282C>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.258C>A
  hgvsp: ENSP00000438357.1:p.Tyr86Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.378C>A
  hgvsp: ENSP00000443548.1:p.Tyr126Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.327C>A
  hgvsp: ENSP00000440016.1:p.Tyr109Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.465C>A
  hgvsp: ENSP00000445657.1:p.Tyr155Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+651C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.258C>A
  hgvsp: ENSP00000442414.1:p.Tyr86Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.465C>A
  hgvsp: ENSP00000438792.1:p.Tyr155Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.465C>A
  hgvsp: ENSP00000443597.1:p.Tyr155Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000444027
  ensembl transcript: ENST00000400925
  gene symbol: STARD10
  hgvsc: ENST00000400925.2:c.4C>A
  hgvsp: ENSP00000444027.1:p.Tyr2Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.465C>A
  hgvsp: ENSP00000335247.6:p.Tyr155Ter
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.186C>A
  hgvsp: ENSP00000445708.1:p.Tyr62Ter
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Tyr155Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

11-72468925-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468925
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468925
    reference: chr 11
allele count: 1
allele frequency: 8.29531314807134e-6
allele num: 120550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.257A>T
  hgvsp: ENSP00000442414.1:p.Tyr86Phe
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.185A>T
  hgvsp: ENSP00000445708.1:p.Tyr62Phe
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.257A>T
  hgvsp: ENSP00000438357.1:p.Tyr86Phe
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.326A>T
  hgvsp: ENSP00000440016.1:p.Tyr109Phe
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.60A>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.464A>T
  hgvsp: ENSP00000438792.1:p.Tyr155Phe
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.464A>T
  hgvsp: ENSP00000445657.1:p.Tyr155Phe
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000444027
  ensembl transcript: ENST00000400925
  gene symbol: STARD10
  hgvsc: ENST00000400925.2:c.3A>T
  hgvsp: ENSP00000444027.1:p.Tyr2Phe
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.464A>T
  hgvsp: ENSP00000443597.1:p.Tyr155Phe
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+650A>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.377A>T
  hgvsp: ENSP00000443548.1:p.Tyr126Phe
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.464A>T
  hgvsp: ENSP00000335247.6:p.Tyr155Phe
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25283A>T
  variant of: http://identifiers.org/hgnc/16925
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr155Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

11-72468932-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468932
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468932
    reference: chr 11
allele count: 6
allele frequency: 4.976527379194798e-5
allele num: 120566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-3C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.53C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25290C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-3C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-3C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-3C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-3C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-3C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-3C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-3C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-3C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+643C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15679
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.460-3C>T
num of homozygotes: 1
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

11-72468934-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468934
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468934
    reference: chr 11
allele count: 1
allele frequency: 8.294487483618387e-6
allele num: 120562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25292C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+641C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-5C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-5C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-5C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-5C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-5C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-5C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-5C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-5C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-5C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.51C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.460-5C>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

11-72468935-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468935
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468935
    reference: chr 11
allele count: 1
allele frequency: 8.294212298657997e-6
allele num: 120566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-6C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-6C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+640C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-6C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-6C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-6C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.50C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-6C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25293C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-6C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-6C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-6C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.460-6C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

11-72468937-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468937
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468937
    reference: chr 11
allele count: 53
allele frequency: 4.396078366317745e-4
allele num: 120562
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+638A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-8A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-8A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-8A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-8A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25295A>G
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-8A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-8A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-8A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-8A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.48A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-8A>G
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 9322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: c.460-8A>G
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

11-72468949-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468949
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468949
    reference: chr 11
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-20C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-20C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-20C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+626C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-20C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-20C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-20C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25307C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-20C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-20C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.36C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-20C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9315
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-72468950-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468950
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468950
    reference: chr 11
allele count: 2
allele frequency: 1.658704883227176e-5
allele num: 120576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.35C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-21C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-21C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-21C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-21C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-21C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-21C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-21C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-21C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+625C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-21C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25308C>T
  variant of: http://identifiers.org/hgnc/16925
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27100
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

11-72468953-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468953
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468953
    reference: chr 11
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.32C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+622C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25311C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-24C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

11-72468962-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468962
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468962
    reference: chr 11
allele count: 6
allele frequency: 4.976692490171033e-5
allele num: 120562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-33C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-33C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-33C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-33C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-33C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-33C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.23C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-33C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+613C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25320C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-33C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-33C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ

11-72468973-AAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468973
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468970
    reference: chr 11
allele count: 158
allele frequency: 1.310768209722914e-3
allele num: 120540
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-47_460-45delCTT
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-47_253-45delCTT
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-47_181-45delCTT
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-47_322-45delCTT
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-47_253-45delCTT
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-47_460-45delCTT
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+599_394+601delCTT
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.9_11delCTT
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-47_460-45delCTT
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25334_-127-25332delCTT
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-47_460-45delCTT
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-47_373-45delCTT
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 15454
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 26727
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9250
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: AAAG
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

11-72468975-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468975
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468975
    reference: chr 11
allele count: 2
allele frequency: 1.663008048958957e-5
allele num: 120264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-46T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.10T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-46T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25333T>C
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-46T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-46T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-46T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+600T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-46T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-46T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-46T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-46T>C
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9242
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

11-72468979-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468979
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468979
    reference: chr 11
allele count: 1
allele frequency: 8.297515723792297e-6
allele num: 120518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-50C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-50C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-50C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.6C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-50C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-50C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-50C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-50C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-50C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+596C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25337C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-50C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

11-72468979-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72468979
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72468979
    reference: chr 11
allele count: 35
allele frequency: 2.904130503327304e-4
allele num: 120518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.253-50C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25337C>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.460-50C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.460-50C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000543089
  gene symbol: STARD10
  hgvsc: ENST00000543089.1:n.6C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.460-50C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.181-50C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.253-50C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.322-50C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+596C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.373-50C>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.460-50C>A
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9237
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26795
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-72469524-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469524
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469524
    reference: chr 11
allele count: 5
allele frequency: 4.562210299645973e-5
allele num: 109596
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25882C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.180+51C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.252+51C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.459+51C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.321+51C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.459+51C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.459+51C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.252+51C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+51C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.372+51C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.459+51C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12575
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16345
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6282
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

11-72469537-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469537
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469537
    reference: chr 11
allele count: 1
allele frequency: 9.086778736937755e-6
allele num: 110050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25895G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.252+38G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.459+38G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.459+38G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.252+38G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.459+38G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.459+38G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.180+38G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.372+38G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.321+38G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+38G>A
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21337
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8079
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-72469542-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469542
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469542
    reference: chr 11
allele count: 2
allele frequency: 1.805966914686123e-5
allele num: 110744
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.459+33G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.459+33G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.180+33G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.321+33G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+33G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25900G>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.252+33G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.252+33G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.372+33G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.459+33G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.459+33G>T
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10322
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4180
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum

11-72469544-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469544
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469544
    reference: chr 11
allele count: 5
allele frequency: 4.511169656068426e-5
allele num: 110836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.459+31C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.180+31C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.459+31C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+31C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.252+31C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.372+31C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.252+31C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.321+31C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25902C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.459+31C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.459+31C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26654
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2517
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

11-72469545-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469545
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469545
    reference: chr 11
allele count: 13
allele frequency: 1.16994852226502e-4
allele num: 111116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.252+30G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.459+30G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.459+30G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.252+30G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.459+30G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.321+30G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+30G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25903G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.180+30G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.459+30G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.372+30G>A
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27304
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11189
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8838
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3308
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

11-72469546-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469546
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469546
    reference: chr 11
allele count: 1
allele frequency: 8.976821845993644e-6
allele num: 111398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+29A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.459+29A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.321+29A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.459+29A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.180+29A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.459+29A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.459+29A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.252+29A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.252+29A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.372+29A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25904A>C
  variant of: http://identifiers.org/hgnc/16925
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

11-72469547-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469547
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469547
    reference: chr 11
allele count: 1
allele frequency: 8.964429145152036e-6
allele num: 111552
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.252+28G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.459+28G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.459+28G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.180+28G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.321+28G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.252+28G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+28G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.372+28G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.459+28G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25905G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.459+28G>A
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28745
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

11-72469548-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469548
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469548
    reference: chr 11
allele count: 2
allele frequency: 1.789773235731033e-5
allele num: 111746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.321+27G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+27G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.459+27G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.180+27G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25906G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.459+27G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.252+27G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.252+27G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.372+27G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.459+27G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.459+27G>A
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29278
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

11-72469551-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469551
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469551
    reference: chr 11
allele count: 1
allele frequency: 8.898538859919202e-6
allele num: 112378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.459+24G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.180+24G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.321+24G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.372+24G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.252+24G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.459+24G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+24G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.252+24G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.459+24G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25909G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.459+24G>A
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2271
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS

11-72469552-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469552
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469552
    reference: chr 11
allele count: 3
allele frequency: 2.668279493382667e-5
allele num: 112432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.459+23C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25910C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.180+23C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.321+23C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.459+23C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.459+23C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.372+23C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.459+23C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.252+23C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+23C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.252+23C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30236
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2833
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

11-72469566-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469566
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469566
    reference: chr 11
allele count: 1
allele frequency: 8.602594542514021e-6
allele num: 116244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.459+9A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.459+9A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25924A>C
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.459+9A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.372+9A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.459+9A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.252+9A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.394+9A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.252+9A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.321+9A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.180+9A>C
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15318
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

11-72469580-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469580
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469580
    reference: chr 11
allele count: 1
allele frequency: 8.462241478522831e-6
allele num: 118172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.454C>T
  hgvsp: ENSP00000438792.1:p.His152Tyr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.454C>T
  hgvsp: ENSP00000443597.1:p.His152Tyr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.175C>T
  hgvsp: ENSP00000445708.1:p.His59Tyr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.454C>T
  hgvsp: ENSP00000445657.1:p.His152Tyr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.316C>T
  hgvsp: ENSP00000440016.1:p.His106Tyr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.367C>T
  hgvsp: ENSP00000443548.1:p.His123Tyr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.454C>T
  hgvsp: ENSP00000335247.6:p.His152Tyr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.247C>T
  hgvsp: ENSP00000438357.1:p.His83Tyr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.247C>T
  hgvsp: ENSP00000442414.1:p.His83Tyr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.389C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25938C>T
  variant of: http://identifiers.org/hgnc/16925
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His152Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ

11-72469590-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469590
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469590
    reference: chr 11
allele count: 5
allele frequency: 4.208258286060565e-5
allele num: 118814
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.444C>T
  hgvsp: ENST00000543304.1:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25948C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.237C>T
  hgvsp: ENST00000544767.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.444C>T
  hgvsp: ENST00000334805.6:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.165C>T
  hgvsp: ENST00000537351.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.379C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.444C>T
  hgvsp: ENST00000542989.1:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.306C>T
  hgvsp: ENST00000538536.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.357C>T
  hgvsp: ENST00000545082.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.444C>T
  hgvsp: ENST00000537947.1:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.237C>T
  hgvsp: ENST00000536728.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3319
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16683
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr148Tyr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

11-72469613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469613
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469613
    reference: chr 11
allele count: 5
allele frequency: 4.195757250268529e-5
allele num: 119168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.421G>A
  hgvsp: ENSP00000445657.1:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.421G>A
  hgvsp: ENSP00000443597.1:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.214G>A
  hgvsp: ENSP00000438357.1:p.Ala72Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.214G>A
  hgvsp: ENSP00000442414.1:p.Ala72Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.142G>A
  hgvsp: ENSP00000445708.1:p.Ala48Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.283G>A
  hgvsp: ENSP00000440016.1:p.Ala95Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.356G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.421G>A
  hgvsp: ENSP00000438792.1:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.421G>A
  hgvsp: ENSP00000335247.6:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25971G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.334G>A
  hgvsp: ENSP00000443548.1:p.Ala112Thr
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala141Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

11-72469614-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469614
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469614
    reference: chr 11
allele count: 2
allele frequency: 1.677908654652841e-5
allele num: 119196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.282C>T
  hgvsp: ENST00000538536.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.355C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.420C>T
  hgvsp: ENST00000537947.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25972C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.420C>T
  hgvsp: ENST00000543304.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.333C>T
  hgvsp: ENST00000545082.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.213C>T
  hgvsp: ENST00000536728.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.420C>T
  hgvsp: ENST00000542989.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.420C>T
  hgvsp: ENST00000334805.6:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.213C>T
  hgvsp: ENST00000544767.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.141C>T
  hgvsp: ENST00000537351.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly140Gly
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

11-72469619-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469619
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469619
    reference: chr 11
allele count: 7
allele frequency: 5.873271580077863e-5
allele num: 119184
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.208A>G
  hgvsp: ENSP00000438357.1:p.Met70Val
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.208A>G
  hgvsp: ENSP00000442414.1:p.Met70Val
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.415A>G
  hgvsp: ENSP00000445657.1:p.Met139Val
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.328A>G
  hgvsp: ENSP00000443548.1:p.Met110Val
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.415A>G
  hgvsp: ENSP00000443597.1:p.Met139Val
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.415A>G
  hgvsp: ENSP00000438792.1:p.Met139Val
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25977A>G
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.136A>G
  hgvsp: ENSP00000445708.1:p.Met46Val
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.277A>G
  hgvsp: ENSP00000440016.1:p.Met93Val
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.415A>G
  hgvsp: ENSP00000335247.6:p.Met139Val
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.350A>G
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met139Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

11-72469622-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469622
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469622
    reference: chr 11
allele count: 1
allele frequency: 8.39630562552477e-6
allele num: 119100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.205C>T
  hgvsp: ENSP00000438357.1:p.Pro69Ser
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.274C>T
  hgvsp: ENSP00000440016.1:p.Pro92Ser
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.412C>T
  hgvsp: ENSP00000438792.1:p.Pro138Ser
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25980C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.205C>T
  hgvsp: ENSP00000442414.1:p.Pro69Ser
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.347C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.325C>T
  hgvsp: ENSP00000443548.1:p.Pro109Ser
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.133C>T
  hgvsp: ENSP00000445708.1:p.Pro45Ser
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.412C>T
  hgvsp: ENST00000546314.1:c.412C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.412C>T
  hgvsp: ENSP00000445657.1:p.Pro138Ser
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.412C>T
  hgvsp: ENSP00000443597.1:p.Pro138Ser
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.412C>T
  hgvsp: ENSP00000335247.6:p.Pro138Ser
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro138Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

11-72469633-C-CG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469633
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469634
    reference: chr 11
allele count: 1
allele frequency: 8.405904307185366e-6
allele num: 118964
alternate allele: CG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.262dupC
  hgvsp: ENSP00000440016.1:p.Arg88ProfsTer9
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.400dupC
  hgvsp: ENSP00000335247.6:p.Arg134ProfsTer9
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.400dupC
  hgvsp: ENSP00000438792.1:p.Arg134ProfsTer9
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.335dupC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25992dupC
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.313dupC
  hgvsp: ENSP00000443548.1:p.Arg105ProfsTer9
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.400dupC
  hgvsp: ENSP00000445886.1:p.Arg134ProfsTer?
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.193dupC
  hgvsp: ENSP00000438357.1:p.Arg65ProfsTer9
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.400dupC
  hgvsp: ENSP00000445657.1:p.Arg134ProfsTer9
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.193dupC
  hgvsp: ENSP00000442414.1:p.Arg65ProfsTer9
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.121dupC
  hgvsp: ENSP00000445708.1:p.Arg41ProfsTer9
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.400dupC
  hgvsp: ENSP00000443597.1:p.Arg134ProfsTer9
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg134ProfsTer9
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

11-72469633-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469633
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469633
    reference: chr 11
allele count: 2
allele frequency: 1.681180861437073e-5
allele num: 118964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.401G>A
  hgvsp: ENSP00000443597.1:p.Arg134His
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.401G>A
  hgvsp: ENSP00000438792.1:p.Arg134His
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.401G>A
  hgvsp: ENSP00000445886.1:p.Arg134His
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.122G>A
  hgvsp: ENSP00000445708.1:p.Arg41His
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.314G>A
  hgvsp: ENSP00000443548.1:p.Arg105His
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25991G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.194G>A
  hgvsp: ENSP00000438357.1:p.Arg65His
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.401G>A
  hgvsp: ENSP00000445657.1:p.Arg134His
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.401G>A
  hgvsp: ENSP00000335247.6:p.Arg134His
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.263G>A
  hgvsp: ENSP00000440016.1:p.Arg88His
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.194G>A
  hgvsp: ENSP00000442414.1:p.Arg65His
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.336G>A
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg134His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

11-72469634-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469634
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469634
    reference: chr 11
allele count: 3
allele frequency: 2.522704339051463e-5
allele num: 118920
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.313C>T
  hgvsp: ENSP00000443548.1:p.Arg105Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.121C>T
  hgvsp: ENSP00000445708.1:p.Arg41Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.400C>T
  hgvsp: ENSP00000335247.6:p.Arg134Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.335C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-25992C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.400C>T
  hgvsp: ENSP00000445657.1:p.Arg134Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.400C>T
  hgvsp: ENSP00000438792.1:p.Arg134Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.193C>T
  hgvsp: ENSP00000438357.1:p.Arg65Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.400C>T
  hgvsp: ENSP00000445886.1:p.Arg134Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.193C>T
  hgvsp: ENSP00000442414.1:p.Arg65Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.262C>T
  hgvsp: ENSP00000440016.1:p.Arg88Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.400C>T
  hgvsp: ENSP00000443597.1:p.Arg134Cys
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg134Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

11-72469642-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469642
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469642
    reference: chr 11
allele count: 1
allele frequency: 8.424174009738345e-6
allele num: 118706
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.254T>C
  hgvsp: ENSP00000440016.1:p.Ile85Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.185T>C
  hgvsp: ENSP00000438357.1:p.Ile62Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.327T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.392T>C
  hgvsp: ENSP00000438792.1:p.Ile131Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.392T>C
  hgvsp: ENSP00000443597.1:p.Ile131Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.305T>C
  hgvsp: ENSP00000443548.1:p.Ile102Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.392T>C
  hgvsp: ENSP00000445886.1:p.Ile131Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.392T>C
  hgvsp: ENSP00000335247.6:p.Ile131Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.392T>C
  hgvsp: ENSP00000445657.1:p.Ile131Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.185T>C
  hgvsp: ENSP00000442414.1:p.Ile62Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.113T>C
  hgvsp: ENSP00000445708.1:p.Ile38Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26000T>C
  variant of: http://identifiers.org/hgnc/16925
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile131Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

11-72469646-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469646
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469646
    reference: chr 11
allele count: 1
allele frequency: 8.441098018030185e-6
allele num: 118468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.388G>A
  hgvsp: ENSP00000443597.1:p.Val130Ile
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.301G>A
  hgvsp: ENSP00000443548.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.388G>A
  hgvsp: ENSP00000445886.1:p.Val130Ile
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.181G>A
  hgvsp: ENSP00000438357.1:p.Val61Ile
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.323G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.109G>A
  hgvsp: ENSP00000445708.1:p.Val37Ile
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26004G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.181G>A
  hgvsp: ENSP00000442414.1:p.Val61Ile
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.250G>A
  hgvsp: ENSP00000440016.1:p.Val84Ile
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.388G>A
  hgvsp: ENSP00000438792.1:p.Val130Ile
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.388G>A
  hgvsp: ENSP00000335247.6:p.Val130Ile
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.388G>A
  hgvsp: ENSP00000445657.1:p.Val130Ile
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val130Ile
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

11-72469652-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469652
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469652
    reference: chr 11
allele count: 1
allele frequency: 8.477737461426295e-6
allele num: 117956
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.295C>T
  hgvsp: ENSP00000443548.1:p.Arg99Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.382C>T
  hgvsp: ENSP00000445657.1:p.Arg128Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.244C>T
  hgvsp: ENSP00000440016.1:p.Arg82Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.382C>T
  hgvsp: ENSP00000335247.6:p.Arg128Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.317C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.175C>T
  hgvsp: ENSP00000442414.1:p.Arg59Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.382C>T
  hgvsp: ENSP00000438792.1:p.Arg128Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26010C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.175C>T
  hgvsp: ENSP00000438357.1:p.Arg59Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.103C>T
  hgvsp: ENSP00000445708.1:p.Arg35Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.382C>T
  hgvsp: ENSP00000443597.1:p.Arg128Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.382C>T
  hgvsp: ENSP00000445886.1:p.Arg128Cys
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35035
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg128Cys
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-72469675-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469675
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469675
    reference: chr 11
allele count: 1
allele frequency: 8.767930417704205e-6
allele num: 114052
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.359G>T
  hgvsp: ENSP00000335247.6:p.Arg120Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.221G>T
  hgvsp: ENSP00000440016.1:p.Arg74Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26033G>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.152G>T
  hgvsp: ENSP00000438357.1:p.Arg51Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.359G>T
  hgvsp: ENSP00000443597.1:p.Arg120Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.359G>T
  hgvsp: ENSP00000438792.1:p.Arg120Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.359G>T
  hgvsp: ENSP00000445657.1:p.Arg120Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.80G>T
  hgvsp: ENSP00000445708.1:p.Arg27Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.272G>T
  hgvsp: ENSP00000443548.1:p.Arg91Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.359G>T
  hgvsp: ENSP00000445886.1:p.Arg120Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.294G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.152G>T
  hgvsp: ENSP00000442414.1:p.Arg51Met
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg120Met
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

11-72469682-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469682
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469682
    reference: chr 11
allele count: 2
allele frequency: 1.79057441627274e-5
allele num: 111696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.218-4A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.77-4A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.269-4A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.149-4A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.291-4A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.356-4A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.149-4A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.356-4A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.356-4A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.356-4A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.356-4A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26040A>C
  variant of: http://identifiers.org/hgnc/16925
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25809
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.356-4A>C
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

11-72469682-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469682
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469683
    reference: chr 11
allele count: 1
allele frequency: 8.952872081363702e-6
allele num: 111696
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.149-5dupC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.356-5dupC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.269-5dupC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.291-5dupC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.356-5dupC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.149-5dupC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.356-5dupC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.218-5dupC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26041dupC
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.356-5dupC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.77-5dupC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.356-5dupC
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13877
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.356-5dupC
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum

11-72469682-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469682
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469681
    reference: chr 11
allele count: 4
allele frequency: 3.581148832545481e-5
allele num: 111696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.356-5delC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.218-5delC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.149-5delC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.269-5delC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.149-5delC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.356-5delC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.291-5delC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.77-5delC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26041delC
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.356-5delC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.356-5delC
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.356-5delC
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.356-5delC
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: TG
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

11-72469687-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469687
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469687
    reference: chr 11
allele count: 1
allele frequency: 9.043063066321825e-6
allele num: 110582
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.356-9C>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.77-9C>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.356-9C>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.269-9C>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.218-9C>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.356-9C>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26045C>G
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.291-9C>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.149-9C>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.356-9C>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.356-9C>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.149-9C>G
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3958
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-72469697-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469697
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469697
    reference: chr 11
allele count: 1
allele frequency: 9.283154787322924e-6
allele num: 107722
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.356-19T>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.218-19T>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.149-19T>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.356-19T>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26055T>G
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.356-19T>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.356-19T>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.269-19T>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.291-19T>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.149-19T>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.77-19T>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.356-19T>G
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7508
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16647
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

11-72469701-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72469701
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72469701
    reference: chr 11
allele count: 1
allele frequency: 9.391082228315991e-6
allele num: 106484
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.269-23G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.218-23G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.356-23G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.149-23G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.356-23G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.77-23G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.291-23G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26059G>C
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.356-23G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.356-23G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.149-23G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.356-23G>C
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8114
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9080
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-72470230-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470230
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470230
    reference: chr 11
allele count: 1
allele frequency: 9.357688276688127e-6
allele num: 106864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26588G>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+49G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+49G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+49G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+49G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+49G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+49G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+49G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+49G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+49G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+49G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+49G>T
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16208
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

11-72470230-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470230
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470230
    reference: chr 11
allele count: 2
allele frequency: 1.871537655337625e-5
allele num: 106864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+49G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+49G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+49G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+49G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+49G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+49G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+49G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+49G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+49G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+49G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+49G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26588G>C
  variant of: http://identifiers.org/hgnc/16925
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16208
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16238
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

11-72470235-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470235
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470235
    reference: chr 11
allele count: 1
allele frequency: 9.291780490977681e-6
allele num: 107622
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+44T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+44T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+44T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+44T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+44T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+44T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+44T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+44T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26593T>C
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+44T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+44T>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+44T>C
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12180
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

11-72470242-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470242
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470242
    reference: chr 11
allele count: 1
allele frequency: 9.231394125140779e-6
allele num: 108326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+37G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+37G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26600G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+37G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.576G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+37G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+37G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+37G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+37G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+37G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+37G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+37G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+37G>A
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

11-72470255-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470255
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470255
    reference: chr 11
allele count: 6
allele frequency: 5.432322317790856e-5
allele num: 110450
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.563C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26613C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+24C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+24C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9123
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27995
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-72470261-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470261
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470261
    reference: chr 11
allele count: 1
allele frequency: 8.961858330943504e-6
allele num: 111584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26619G>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+18G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+18G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+18G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.557G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+18G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+18G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+18G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+18G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+18G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+18G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+18G>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+18G>T
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30428
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

11-72470261-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470261
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470261
    reference: chr 11
allele count: 1
allele frequency: 8.961858330943504e-6
allele num: 111584
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.557G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26619G>C
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+18G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+18G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+18G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+18G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+18G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+18G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+18G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+18G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+18G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+18G>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+18G>C
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30428
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS

11-72470261-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470261
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470261
    reference: chr 11
allele count: 3
allele frequency: 2.688557499283051e-5
allele num: 111584
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26619G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+18G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+18G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+18G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+18G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+18G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+18G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.557G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+18G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+18G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+18G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+18G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+18G>A
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8407
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

11-72470262-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470262
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470262
    reference: chr 11
allele count: 6
allele frequency: 5.350550214913767e-5
allele num: 112138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+17C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+17C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+17C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+17C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+17C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26620C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+17C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+17C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.556C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+17C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+17C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+17C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+17C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31210
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-72470266-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470266
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470266
    reference: chr 11
allele count: 1
allele frequency: 8.823788934968676e-6
allele num: 113330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+13A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.552A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+13A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+13A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+13A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+13A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26624A>G
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+13A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+13A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+13A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+13A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+13A>G
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+13A>G
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-72470268-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470268
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470268
    reference: chr 11
allele count: 831
allele frequency: 7.300488456267351e-3
allele num: 113828
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26626G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+11G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+11G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+11G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+11G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+11G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+11G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+11G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.550G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+11G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+11G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+11G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+11G>A
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 3.25e1
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 9696
  bin: 2.75e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 32946
  bin: 2.25e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 3.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 1.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 1.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
num of homozygotes: 3
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

11-72470269-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470269
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470269
    reference: chr 11
allele count: 3
allele frequency: 2.624488224796165e-5
allele num: 114308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+10C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26627C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+10C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+10C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+10C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+10C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+10C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+10C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+10C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+10C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+10C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.549C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+10C>T
  variant of: http://identifiers.org/hgnc/10666
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9921
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

11-72470272-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470272
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470272
    reference: chr 11
allele count: 2
allele frequency: 1.732922053166049e-5
allele num: 115412
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.355+7A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.290+7A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.355+7A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.355+7A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.268+7A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.76+7A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.355+7A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.148+7A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.148+7A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.355+7A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26630A>C
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.217+7A>C
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.546A>C
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.355+7A>C
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

11-72470290-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470290
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470290
    reference: chr 11
allele count: 1
allele frequency: 8.429997302400863e-6
allele num: 118624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.344G>A
  hgvsp: ENSP00000445886.1:p.Gly115Asp
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.344G>A
  hgvsp: ENSP00000445657.1:p.Gly115Asp
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.279G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.344G>A
  hgvsp: ENSP00000335247.6:p.Gly115Asp
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.528G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26648G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.137G>A
  hgvsp: ENSP00000438357.1:p.Gly46Asp
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.65G>A
  hgvsp: ENSP00000445708.1:p.Gly22Asp
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.206G>A
  hgvsp: ENSP00000440016.1:p.Gly69Asp
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.344G>A
  hgvsp: ENSP00000438792.1:p.Gly115Asp
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.137G>A
  hgvsp: ENSP00000442414.1:p.Gly46Asp
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.344G>A
  hgvsp: ENSP00000443597.1:p.Gly115Asp
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.257G>A
  hgvsp: ENSP00000443548.1:p.Gly86Asp
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly115Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

11-72470294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470294
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470294
    reference: chr 11
allele count: 17
allele frequency: 1.426581407448433e-4
allele num: 119166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.133G>A
  hgvsp: ENSP00000442414.1:p.Val45Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.524G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.340G>A
  hgvsp: ENSP00000438792.1:p.Val114Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.61G>A
  hgvsp: ENSP00000445708.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.133G>A
  hgvsp: ENSP00000438357.1:p.Val45Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.340G>A
  hgvsp: ENSP00000445886.1:p.Val114Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.340G>A
  hgvsp: ENSP00000443597.1:p.Val114Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.253G>A
  hgvsp: ENSP00000443548.1:p.Val85Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.340G>A
  hgvsp: ENSP00000445657.1:p.Val114Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.340G>A
  hgvsp: ENSP00000335247.6:p.Val114Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.202G>A
  hgvsp: ENSP00000440016.1:p.Val68Met
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26652G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.275G>A
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35821
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val114Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-72470295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470295
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470295
    reference: chr 11
allele count: 1
allele frequency: 8.378156470450242e-6
allele num: 119358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.339C>T
  hgvsp: ENST00000537947.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.252C>T
  hgvsp: ENST00000545082.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.339C>T
  hgvsp: ENST00000546314.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.339C>T
  hgvsp: ENST00000542989.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.274C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.339C>T
  hgvsp: ENST00000543304.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.523C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.201C>T
  hgvsp: ENST00000538536.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.60C>T
  hgvsp: ENST00000537351.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.339C>T
  hgvsp: ENST00000334805.6:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.132C>T
  hgvsp: ENST00000536728.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26653C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.132C>T
  hgvsp: ENST00000544767.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp113Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

11-72470300-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470300
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470300
    reference: chr 11
allele count: 3
allele frequency: 2.504299046696829e-5
allele num: 119794
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.334G>A
  hgvsp: ENSP00000335247.6:p.Ala112Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.334G>A
  hgvsp: ENSP00000438792.1:p.Ala112Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.196G>A
  hgvsp: ENSP00000440016.1:p.Ala66Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.334G>A
  hgvsp: ENSP00000445657.1:p.Ala112Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26658G>A
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.334G>A
  hgvsp: ENSP00000443597.1:p.Ala112Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.269G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.55G>A
  hgvsp: ENSP00000445708.1:p.Ala19Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.127G>A
  hgvsp: ENSP00000438357.1:p.Ala43Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.334G>A
  hgvsp: ENSP00000445886.1:p.Ala112Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.247G>A
  hgvsp: ENSP00000443548.1:p.Ala83Thr
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.518G>A
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.127G>A
  hgvsp: ENSP00000442414.1:p.Ala43Thr
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala112Thr
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

11-72470301-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470301
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470301
    reference: chr 11
allele count: 8
allele frequency: 6.671670419481278e-5
allele num: 119910
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.333C>T
  hgvsp: ENST00000334805.6:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.268C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.333C>T
  hgvsp: ENST00000546314.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.195C>T
  hgvsp: ENST00000538536.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.517C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.333C>T
  hgvsp: ENST00000542989.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.333C>T
  hgvsp: ENST00000543304.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.333C>T
  hgvsp: ENST00000537947.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.126C>T
  hgvsp: ENST00000544767.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.54C>T
  hgvsp: ENST00000537351.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000441589
  ensembl transcript: ENST00000539138
  gene symbol: STARD10
  hgvsc: ENST00000539138.1:c.246C>T
  hgvsp: ENST00000539138.1:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26659C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.246C>T
  hgvsp: ENST00000545082.1:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.126C>T
  hgvsp: ENST00000536728.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn111Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

11-72470315-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72470315
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 72470315
    reference: chr 11
allele count: 1
allele frequency: 8.29985724245543e-6
allele num: 120484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000535267
  gene symbol: STARD10
  hgvsc: ENST00000535267.1:n.503C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443548
  ensembl transcript: ENST00000545082
  gene symbol: STARD10
  hgvsc: ENST00000545082.1:c.232C>T
  hgvsp: ENSP00000443548.1:p.Arg78Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000442414
  ensembl transcript: ENST00000536728
  gene symbol: STARD10
  hgvsc: ENST00000536728.1:c.112C>T
  hgvsp: ENSP00000442414.1:p.Arg38Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438357
  ensembl transcript: ENST00000544767
  gene symbol: STARD10
  hgvsc: ENST00000544767.1:c.112C>T
  hgvsp: ENSP00000438357.1:p.Arg38Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000441589
  ensembl transcript: ENST00000539138
  gene symbol: STARD10
  hgvsc: ENST00000539138.1:c.232C>T
  hgvsp: ENSP00000441589.1:p.Arg78Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445657
  ensembl transcript: ENST00000537947
  gene symbol: STARD10
  hgvsc: ENST00000537947.1:c.319C>T
  hgvsp: ENSP00000445657.1:p.Arg107Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000440016
  ensembl transcript: ENST00000538536
  gene symbol: STARD10
  hgvsc: ENST00000538536.1:c.181C>T
  hgvsp: ENSP00000440016.1:p.Arg61Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214530
  ensembl transcript: ENST00000538437
  gene symbol: STARD10
  hgvsc: ENST00000538437.1:n.254C>T
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000438792
  ensembl transcript: ENST00000543304
  gene symbol: STARD10
  hgvsc: ENST00000543304.1:c.319C>T
  hgvsp: ENSP00000438792.1:p.Arg107Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445886
  ensembl transcript: ENST00000546314
  gene symbol: STARD10
  hgvsc: ENST00000546314.1:c.319C>T
  hgvsp: ENSP00000445886.1:p.Arg107Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000443597
  ensembl transcript: ENST00000542989
  gene symbol: STARD10
  hgvsc: ENST00000542989.1:c.319C>T
  hgvsp: ENSP00000443597.1:p.Arg107Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186635
  ensembl protein: ENSP00000352332
  ensembl transcript: ENST00000359373
  gene symbol: ARAP1
  hgvsc: ENST00000359373.5:c.-127-26673C>T
  variant of: http://identifiers.org/hgnc/16925
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000335247
  ensembl transcript: ENST00000334805
  gene symbol: STARD10
  hgvsc: ENST00000334805.6:c.319C>T
  hgvsp: ENSP00000335247.6:p.Arg107Cys
  variant of: http://identifiers.org/hgnc/10666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214530
  ensembl protein: ENSP00000445708
  ensembl transcript: ENST00000537351
  gene symbol: STARD10
  hgvsc: ENST00000537351.1:c.40C>T
  hgvsp: ENSP00000445708.1:p.Arg14Cys
  variant of: http://identifiers.org/hgnc/10666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg107Cys
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 115
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 413
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1635
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5877
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3957
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 5378
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9059
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4234
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1778
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.703902e6

QD
type: SiteQuality
SIO_000300: 1.207e1

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.51e-1

FS
type: SiteQuality
SIO_000300: 3.158e0

MQRankSum
type: SiteQuality
SIO_000300: 2.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

GenotypeDepth
all individuals: 15652
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 871
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4234
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9059
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1778
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5378
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3957
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5877
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27714
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502584445245823e-5
allele num: 66552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

DP
type: SiteQuality
SIO_000300: 1.703902e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 3.158e0

VQSLOD
type: SiteQuality
SIO_000300: -1.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e0

QD
type: SiteQuality
SIO_000300: 1.207e1

GenotypeDepth
all individuals: 115
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 448
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 414
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 872
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27679
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3962
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9057
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5879
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4240
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502268425322237e-5
allele num: 66566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.488e0

FS
type: SiteQuality
SIO_000300: 4.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.48e-1

MQ
type: SiteQuality
SIO_000300: 5.9e1

MQRankSum
type: SiteQuality
SIO_000300: -1.228e0

QD
type: SiteQuality
SIO_000300: 6.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.393e0

DP
type: SiteQuality
SIO_000300: 1.704461e6

GenotypeDepth
all individuals: 3305
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 872
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27212
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27645
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4245
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3965
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5880
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9063
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1780
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5382
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
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Latino
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South Asian
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allele frequency: 0.0e0
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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: 1.502087902184036e-5
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66570
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African
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Other
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European (Finnish)
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East Asian
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Latino
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VQSLOD
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BaseQRankSum
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MQ
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FS
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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African
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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ReadPosRankSum
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DP
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ClippingRankSum
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QD
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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East Asian
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African
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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: 9.010903192863365e-5
allele num: 66586
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European (Finnish)
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BaseQRankSum
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QD
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MQ
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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DP
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ReadPosRankSum
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SIO_000300: 6.45e-1

GenotypeDepth
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variant carriers: 0

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

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

Latino
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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

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

ClippingRankSum
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SIO_000300: -1.423e0

FS
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SIO_000300: 0.0e0

MQ
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SIO_000300: 5.883e1

QD
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MQRankSum
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SIO_000300: -2.09e-1

DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -9.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
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

Other
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allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-1

BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.2e-3

MQ
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SIO_000300: 5.918e1

QD
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SIO_000300: 1.244e1

FS
type: SiteQuality
SIO_000300: 8.839e0

MQRankSum
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SIO_000300: 5.26e-1

DP
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SIO_000300: 1.708207e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 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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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

African
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

QD
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DP
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BaseQRankSum
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FS
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SIO_000300: 1.22e0

MQ
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SIO_000300: 5.963e1

VQSLOD
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ClippingRankSum
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SIO_000300: -5.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.06e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

African
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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: 6
allele frequency: 9.011715229798738e-5
allele num: 66580
num of homozygotes: 0

Other
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 1.6e-3

MQRankSum
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BaseQRankSum
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SIO_000300: -6.09e-1

ReadPosRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -9.0e-2

DP
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QD
type: SiteQuality
SIO_000300: 1.382e1

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6090
bin: 9.75e1
variant carriers: 158

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

African
type: Population
allele count: 145
allele frequency: 1.479893855888957e-2
allele num: 9798
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502042778178322e-5
allele num: 66576
num of homozygotes: 0

Latino
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allele frequency: 9.505703422053232e-4
allele num: 11572
num of homozygotes: 0

Other
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BaseQRankSum
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SIO_000300: 6.19e-1

VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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MQRankSum
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FS
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ClippingRankSum
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SIO_000300: -1.8e-2

QD
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GenotypeDepth
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variant carriers: 0

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

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

Other
type: Population
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Latino
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East Asian
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South Asian
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allele frequency: 1.212268153715602e-4
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European (Non-Finnish)
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European (Finnish)
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MQ
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ClippingRankSum
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DP
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InbreedingCoeff
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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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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 1.020616452337212e-4
allele num: 9798
num of homozygotes: 0

European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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ReadPosRankSum
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MQRankSum
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QD
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 35

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 1.940334707737085e-3
allele num: 16492
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004446580939791e-5
allele num: 66568
num of homozygotes: 0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.471e0

BaseQRankSum
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SIO_000300: -3.25e0

InbreedingCoeff
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SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.142e1

DP
type: SiteQuality
SIO_000300: 1.711726e6

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7716
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.860031104199067e-4
allele num: 10288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15368
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61162
num of homozygotes: 0

QD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.144e0

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.49e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61240
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15478
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.593246354566385e-5
allele num: 10424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8668
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5564
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.211788e6

VQSLOD
type: SiteQuality
SIO_000300: -1.862e0

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.021e0

QD
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SIO_000300: 5.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

GenotypeQuality
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variant carriers: 1

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7926
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.503896597605019e-5
allele num: 10522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.622007396353727e-5
allele num: 61652
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.247532e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.662e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

QD
type: SiteQuality
SIO_000300: 2.96e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8734
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7950
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.101626806662777e-5
allele num: 61716
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5602
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

BaseQRankSum
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SIO_000300: -3.366e0

DP
type: SiteQuality
SIO_000300: 1.263875e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.464750945469826e-5
allele num: 61874
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 8.516275548826646e-4
allele num: 10568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7974
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.271981e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.611707442864971e-5
allele num: 62046
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5608
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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BaseQRankSum
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.943e1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.609943008017516e-5
allele num: 62114
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
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5620
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.21450384133209e-5
allele num: 62218
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8822
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5628
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 10642
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

DP
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SIO_000300: 1.297665e6

InbreedingCoeff
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SIO_000300: -9.0e-4

ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -4.01e-1

ClippingRankSum
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SIO_000300: -1.234e0

QD
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SIO_000300: 1.593e1

FS
type: SiteQuality
SIO_000300: 2.768e0

MQRankSum
type: SiteQuality
SIO_000300: -4.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.598005688900252e-5
allele num: 62578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8112
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5666
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8848
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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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MQRankSum
type: SiteQuality
SIO_000300: 6.68e-1

ReadPosRankSum
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DP
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SIO_000300: 1.319952e6

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

ClippingRankSum
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SIO_000300: -1.9e-2

BaseQRankSum
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SIO_000300: -2.807e0

QD
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SIO_000300: 6.99e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.877e-1

FS
type: SiteQuality
SIO_000300: 2.663e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.597495127639861e-5
allele num: 62598
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.321401938851603e-5
allele num: 10728
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5654
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.21654501216545e-3
allele num: 822
num of homozygotes: 0

South Asian
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: 8864
num of homozygotes: 0

FS
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SIO_000300: 1.362e0

QD
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BaseQRankSum
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MQ
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VQSLOD
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SIO_000300: 1.01e0

ClippingRankSum
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SIO_000300: -7.8e-2

DP
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SIO_000300: 1.330709e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 703
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15960
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.180916391119509e-4
allele num: 8468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.276e1

InbreedingCoeff
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SIO_000300: -4.0e-4

MQRankSum
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ClippingRankSum
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SIO_000300: -7.25e-1

MQ
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SIO_000300: 5.928e1

VQSLOD
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SIO_000300: 1.15e0

BaseQRankSum
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SIO_000300: 1.97e0

FS
type: SiteQuality
SIO_000300: 1.128e0

ReadPosRankSum
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SIO_000300: 2.04e0

DP
type: SiteQuality
SIO_000300: 1.419451e6

GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6074
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527090587013621e-5
allele num: 65484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
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SIO_000300: 4.41e-1

InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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SIO_000300: -9.78e-1

FS
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SIO_000300: 1.226e0

QD
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SIO_000300: 1.138e1

MQ
type: SiteQuality
SIO_000300: 5.924e1

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65804
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.079002079002079e-4
allele num: 9620
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.835311391166035e-4
allele num: 16346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6134
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
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MQRankSum
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SIO_000300: 1.19e0

ReadPosRankSum
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SIO_000300: 2.53e-1

BaseQRankSum
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FS
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MQ
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SIO_000300: 5.97e1

DP
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VQSLOD
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InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 4.3e-2

QD
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65942
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

East Asian
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allele count: 4
allele frequency: 4.650081376424087e-4
allele num: 8602
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.092360180333861e-5
allele num: 16414
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11494
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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

African
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allele count: 0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 792
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9678
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.031956824934813e-5
allele num: 65964
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.473653e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.749e-1

QD
type: SiteQuality
SIO_000300: 8.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-2

GenotypeDepth
all individuals: 21
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49987
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5018
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.061345786457228e-4
allele num: 65954
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 1.094e0

MQRankSum
type: SiteQuality
SIO_000300: -1.1e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

DP
type: SiteQuality
SIO_000300: 1.473924e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 982
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 790
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variant carriers: 1

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49725
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 1164
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variant carriers: 0

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

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.105006105006105e-5
allele num: 16380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65924
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9678
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.472338e6

QD
type: SiteQuality
SIO_000300: 1.231e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

FS
type: SiteQuality
SIO_000300: 5.008e0

VQSLOD
type: SiteQuality
SIO_000300: -1.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17203
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 966
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49541
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4984
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6134
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.469471e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

MQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 5.863e1

QD
type: SiteQuality
SIO_000300: 8.69e0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49541
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1217
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4984
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.63025758069775e-4
allele num: 6134
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

DP
type: SiteQuality
SIO_000300: 1.469471e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

GenotypeDepth
all individuals: 125
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 77
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 212
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4987
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 5.25e1
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GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 783
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 49406
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.131207847946045e-5
allele num: 16310
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.741250217656277e-4
allele num: 11486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

QD
type: SiteQuality
SIO_000300: 1.337e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.468566e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 553
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
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GenotypeQuality
all individuals: 779
bin: 9.75e1
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GenotypeQuality
all individuals: 272
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 118
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GenotypeQuality
all individuals: 1524
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GenotypeQuality
all individuals: 106
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GenotypeQuality
all individuals: 258
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GenotypeQuality
all individuals: 445
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GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4966
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49143
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1130
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
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GenotypeQuality
all individuals: 151
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519341213649761e-5
allele num: 65818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16220
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.463486e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.63e-1

QD
type: SiteQuality
SIO_000300: 1.187e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 9.45e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeDepth
all individuals: 21
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17156
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
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GenotypeQuality
all individuals: 101
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
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variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 7.5e0
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GenotypeQuality
all individuals: 936
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variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 5.25e1
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GenotypeQuality
all individuals: 4905
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 195
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48545
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6060
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16170
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65718
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.738203425375742e-5
allele num: 11444
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9628
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.23e-1

BaseQRankSum
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MQRankSum
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SIO_000300: -3.93e-1

ReadPosRankSum
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SIO_000300: 8.139999999999999e-1

MQ
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SIO_000300: 5.964e1

DP
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SIO_000300: 1.458185e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
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SIO_000300: 1.128e0

ClippingRankSum
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SIO_000300: -9.79e-1

QD
type: SiteQuality
SIO_000300: 1.109e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9578
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6028
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16018
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65520
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.08e-1

MQ
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SIO_000300: 6.0e1

MQRankSum
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DP
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FS
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -1.48e-1

InbreedingCoeff
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SIO_000300: 4.0e-4

QD
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SIO_000300: 1.328e1

ReadPosRankSum
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SIO_000300: 8.55e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14946
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11030
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

East Asian
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: 9242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.565288169552014e-5
allele num: 63886
num of homozygotes: 0

QD
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SIO_000300: 9.390000000000001e0

FS
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SIO_000300: 4.398e0

BaseQRankSum
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SIO_000300: -3.862e0

InbreedingCoeff
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SIO_000300: 3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

MQRankSum
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SIO_000300: 2.64e-1

DP
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SIO_000300: 1.353919e6

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 6.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.27e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.185220576524925e-5
allele num: 62790
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14414
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.25e-1

QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 5.8e-3

VQSLOD
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ClippingRankSum
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SIO_000300: 9.1e-2

FS
type: SiteQuality
SIO_000300: 7.94e-1

DP
type: SiteQuality
SIO_000300: 1.292258e6

MQRankSum
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SIO_000300: 6.17e-1

BaseQRankSum
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SIO_000300: -1.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

African
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allele frequency: 1.103265666372463e-4
allele num: 9064
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62790
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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FS
type: SiteQuality
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DP
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.25e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 2

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

Other
type: Population
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num of homozygotes: 0

Latino
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allele frequency: 9.257544899092761e-5
allele num: 10802
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 4.777830864787386e-5
allele num: 62790
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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MQRankSum
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GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 5630
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.604518323599255e-5
allele num: 62324
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East Asian
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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FS
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DP
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

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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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61046
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.266464032421479e-4
allele num: 7896
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ClippingRankSum
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SIO_000300: 5.78e-1

BaseQRankSum
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VQSLOD
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QD
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MQRankSum
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FS
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InbreedingCoeff
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SIO_000300: -1.2e-3

ReadPosRankSum
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SIO_000300: -6.830000000000001e-1

DP
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SIO_000300: 1.128078e6

MQ
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GenotypeDepth
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variant carriers: 0

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

African
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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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East Asian
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allele frequency: 1.280081925243216e-4
allele num: 7812
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South Asian
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allele frequency: 0.0e0
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Latino
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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DP
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ClippingRankSum
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QD
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MQRankSum
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SIO_000300: -6.06e-1

MQ
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59772
num of homozygotes: 0

Other
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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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allele frequency: 0.0e0
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African
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ReadPosRankSum
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SIO_000300: 1.68e-1

QD
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DP
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5562
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.182312603452353e-4
allele num: 8458
num of homozygotes: 0

Latino
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South Asian
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num of homozygotes: 0

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: 1.673024158468848e-5
allele num: 59772
num of homozygotes: 0

Other
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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SIO_000300: 8.36e-1

MQRankSum
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SIO_000300: 3.65e-1

QD
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SIO_000300: 6.09e0

DP
type: SiteQuality
SIO_000300: 1.193757e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.663118680149015e-5
allele num: 60128
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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allele frequency: 0.0e0
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South Asian
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Other
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Latino
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ReadPosRankSum
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SIO_000300: 1.59e0

QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Latino
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allele frequency: 1.00341159943809e-4
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European (Finnish)
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Other
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South Asian
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African
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European (Non-Finnish)
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ReadPosRankSum
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QD
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FS
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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East Asian
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Latino
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African
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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BaseQRankSum
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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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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15424
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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8810
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.608337622233659e-5
allele num: 62176
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.43e-1

FS
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SIO_000300: 1.814e0

BaseQRankSum
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ReadPosRankSum
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QD
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SIO_000300: 1.491e1

MQ
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ClippingRankSum
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SIO_000300: -9.85e-1

InbreedingCoeff
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SIO_000300: 1.34e-2

MQRankSum
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SIO_000300: 7.7e-2

DP
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SIO_000300: 1.409602e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8810
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

Other
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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

South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 1.240694789081886e-4
allele num: 8060
num of homozygotes: 0

MQ
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MQRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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DP
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SIO_000300: 1.409602e6

VQSLOD
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SIO_000300: 8.43e-1

FS
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SIO_000300: 1.814e0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8810
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62176
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.296680497925311e-4
allele num: 15424
num of homozygotes: 1

Latino
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allele count: 1
allele frequency: 9.648784253184099e-5
allele num: 10364
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5914
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -1.37e0

InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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FS
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SIO_000300: 1.814e0

MQRankSum
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QD
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SIO_000300: 1.491e1

ReadPosRankSum
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SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.606763161265531e-5
allele num: 62456
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5956
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8854
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 3.675e0

DP
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SIO_000300: 1.422977e6

QD
type: SiteQuality
SIO_000300: 1.354e1

ClippingRankSum
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SIO_000300: -4.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.585389054473968e-5
allele num: 63076
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6064
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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DP
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BaseQRankSum
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MQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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SIO_000300: 6.65e-1

ClippingRankSum
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SIO_000300: -3.61e-1

GenotypeDepth
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variant carriers: 19

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 818

Other
type: Population
allele count: 8
allele frequency: 9.433962264150943e-3
allele num: 848
num of homozygotes: 0

South Asian
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allele frequency: 3.061224489795918e-3
allele num: 15680
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8210
num of homozygotes: 0

European (Non-Finnish)
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allele count: 616
allele frequency: 9.720074478492758e-3
allele num: 63374
num of homozygotes: 3

African
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allele count: 17
allele frequency: 1.894361488745264e-3
allele num: 8974
num of homozygotes: 0

Latino
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allele count: 44
allele frequency: 4.138449962377728e-3
allele num: 10632
num of homozygotes: 0

European (Finnish)
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allele count: 98
allele frequency: 1.60392798690671e-2
allele num: 6110
num of homozygotes: 0

MQRankSum
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SIO_000300: 2.07e-1

ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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FS
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DP
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QD
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SIO_000300: 1.368e1

GenotypeDepth
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.714460822830562e-5
allele num: 63634
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9040
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6144
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South Asian
type: Population
allele count: 0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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VQSLOD
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MQRankSum
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QD
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MQ
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DP
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SIO_000300: 1.486141e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Other
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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FS
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65826
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African
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East Asian
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South Asian
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European (Finnish)
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Other
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MQ
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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Latino
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African
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Other
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East Asian
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European (Non-Finnish)
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ReadPosRankSum
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DP
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

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