1-11718819-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718819
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718819
    reference: chr 1
allele count: 3
allele frequency: 2.492315360970341e-5
allele num: 120370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.486C>T
  hgvsp: ENST00000376768.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.515C>T
  hgvsp: ENSP00000365961.1:p.Ser172Phe
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.161C>T
  hgvsp: ENST00000475435.1:c.161C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.390C>T
  hgvsp: ENST00000376760.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.390C>T
  hgvsp: ENST00000376762.4:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.515C>T
  hgvsp: ENSP00000251547.5:p.Ser172Phe
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.390C>T
  hgvsp: ENST00000425796.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.390C>T
  hgvsp: ENST00000251546.4:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.114C>T
  hgvsp: ENST00000471895.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4205
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser172Phe
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

1-11718822-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718822
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718822
    reference: chr 1
allele count: 1
allele frequency: 8.30592378484335e-6
allele num: 120396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.393A>G
  hgvsp: ENST00000425796.1:c.393A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.393A>G
  hgvsp: ENST00000251546.4:c.393A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.117A>G
  hgvsp: ENST00000471895.1:c.117A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.518A>G
  hgvsp: ENSP00000365961.1:p.Lys173Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.164A>G
  hgvsp: ENST00000475435.1:c.164A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.393A>G
  hgvsp: ENST00000376760.1:c.393A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.489A>G
  hgvsp: ENST00000376768.1:c.489A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.393A>G
  hgvsp: ENST00000376762.4:c.393A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.518A>G
  hgvsp: ENSP00000251547.5:p.Lys173Arg
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2999
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys173Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

1-11718823-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718823
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718823
    reference: chr 1
allele count: 1
allele frequency: 8.306199747491528e-6
allele num: 120392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.394G>C
  hgvsp: ENSP00000251546.4:p.Val132Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.490G>C
  hgvsp: ENSP00000365959.1:p.Val164Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.394G>C
  hgvsp: ENSP00000365951.1:p.Val132Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.519G>C
  hgvsp: ENSP00000365961.1:p.Lys173Asn
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.394G>C
  hgvsp: ENSP00000365953.4:p.Val132Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.165G>C
  hgvsp: ENSP00000473420.1:p.Val56Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.519G>C
  hgvsp: ENSP00000251547.5:p.Lys173Asn
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.394G>C
  hgvsp: ENSP00000389820.1:p.Val132Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.118G>C
  hgvsp: ENSP00000473653.1:p.Val40Leu
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys173Asn
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

1-11718824-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718824
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718824
    reference: chr 1
allele count: 1
allele frequency: 8.305647840531562e-6
allele num: 120400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.395T>C
  hgvsp: ENSP00000389820.1:p.Val132Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.395T>C
  hgvsp: ENSP00000251546.4:p.Val132Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.395T>C
  hgvsp: ENSP00000365951.1:p.Val132Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.520T>C
  hgvsp: ENSP00000365961.1:p.Tyr174His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.520T>C
  hgvsp: ENSP00000251547.5:p.Tyr174His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.119T>C
  hgvsp: ENSP00000473653.1:p.Val40Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.166T>C
  hgvsp: ENSP00000473420.1:p.Val56Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.395T>C
  hgvsp: ENSP00000365953.4:p.Val132Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.491T>C
  hgvsp: ENSP00000365959.1:p.Val164Ala
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2998
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr174His
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

1-11718830-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718830
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718830
    reference: chr 1
allele count: 2
allele frequency: 1.661239949498306e-5
allele num: 120392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.172C>T
  hgvsp: ENSP00000473420.1:p.Ala58Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.401C>T
  hgvsp: ENSP00000251546.4:p.Ala134Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.401C>T
  hgvsp: ENSP00000365953.4:p.Ala134Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.401C>T
  hgvsp: ENSP00000389820.1:p.Ala134Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.526C>T
  hgvsp: ENST00000376770.1:c.526C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.497C>T
  hgvsp: ENSP00000365959.1:p.Ala166Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.401C>T
  hgvsp: ENSP00000365951.1:p.Ala134Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.526C>T
  hgvsp: ENST00000251547.5:c.526C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.125C>T
  hgvsp: ENSP00000473653.1:p.Ala42Val
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5087
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4204
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala42Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

1-11718832-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718832
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718832
    reference: chr 1
allele count: 3
allele frequency: 2.491984117754556e-5
allele num: 120386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.127G>A
  hgvsp: ENSP00000473653.1:p.Val43Met
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.403G>A
  hgvsp: ENSP00000389820.1:p.Val135Met
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.403G>A
  hgvsp: ENSP00000365953.4:p.Val135Met
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.403G>A
  hgvsp: ENSP00000365951.1:p.Val135Met
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.499G>A
  hgvsp: ENSP00000365959.1:p.Val167Met
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.403G>A
  hgvsp: ENSP00000251546.4:p.Val135Met
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.174G>A
  hgvsp: ENSP00000473420.1:p.Val59Met
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.528G>A
  hgvsp: ENST00000251547.5:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.528G>A
  hgvsp: ENST00000376770.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31766
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5087
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val43Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

1-11718833-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718833
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718833
    reference: chr 1
allele count: 1
allele frequency: 8.306889734345666e-6
allele num: 120382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.404T>C
  hgvsp: ENSP00000365953.4:p.Val135Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.404T>C
  hgvsp: ENSP00000251546.4:p.Val135Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.404T>C
  hgvsp: ENSP00000365951.1:p.Val135Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.529T>C
  hgvsp: ENSP00000251547.5:p.Cys177Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.500T>C
  hgvsp: ENSP00000365959.1:p.Val167Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.404T>C
  hgvsp: ENSP00000389820.1:p.Val135Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.529T>C
  hgvsp: ENSP00000365961.1:p.Cys177Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.128T>C
  hgvsp: ENSP00000473653.1:p.Val43Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.175T>C
  hgvsp: ENSP00000473420.1:p.Val59Ala
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4203
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys177Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ

1-11718836-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718836
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718836
    reference: chr 1
allele count: 30
allele frequency: 2.492688114863068e-4
allele num: 120352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.503G>A
  hgvsp: ENSP00000365959.1:p.Arg168His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.407G>A
  hgvsp: ENSP00000251546.4:p.Arg136His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.532G>A
  hgvsp: ENSP00000251547.5:p.Val178Ile
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.407G>A
  hgvsp: ENSP00000365953.4:p.Arg136His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.532G>A
  hgvsp: ENSP00000365961.1:p.Val178Ile
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.407G>A
  hgvsp: ENSP00000389820.1:p.Arg136His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.407G>A
  hgvsp: ENSP00000365951.1:p.Arg136His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.131G>A
  hgvsp: ENSP00000473653.1:p.Arg44His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.178G>A
  hgvsp: ENSP00000473420.1:p.Arg60His
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22995
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9229
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4201
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val178Ile
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

1-11718843-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718843
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718843
    reference: chr 1
allele count: 5
allele frequency: 4.1571053244205e-5
allele num: 120276
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.539T>G
  hgvsp: ENSP00000365961.1:p.Leu180Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.414T>G
  hgvsp: ENST00000425796.1:c.414T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.414T>G
  hgvsp: ENST00000376760.1:c.414T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.510T>G
  hgvsp: ENST00000376768.1:c.510T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.185T>G
  hgvsp: ENST00000475435.1:c.185T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.414T>G
  hgvsp: ENST00000251546.4:c.414T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.539T>G
  hgvsp: ENSP00000251547.5:p.Leu180Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.414T>G
  hgvsp: ENST00000376762.4:c.414T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.138T>G
  hgvsp: ENST00000471895.1:c.138T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu180Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-11718844-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718844
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718844
    reference: chr 1
allele count: 3
allele frequency: 2.494346148729547e-5
allele num: 120272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.415C>A
  hgvsp: ENSP00000365951.1:p.Pro139Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.415C>A
  hgvsp: ENSP00000365953.4:p.Pro139Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.415C>A
  hgvsp: ENSP00000251546.4:p.Pro139Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.511C>A
  hgvsp: ENSP00000365959.1:p.Pro171Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.186C>A
  hgvsp: ENSP00000473420.1:p.Pro63Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.415C>A
  hgvsp: ENSP00000389820.1:p.Pro139Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.139C>A
  hgvsp: ENSP00000473653.1:p.Pro47Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.540C>A
  hgvsp: ENST00000376770.1:c.540C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.540C>A
  hgvsp: ENST00000251547.5:c.540C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5074
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro47Thr
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-11718847-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718847
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718847
    reference: chr 1
allele count: 2
allele frequency: 1.663616702711695e-5
allele num: 120220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.514G>A
  hgvsp: ENSP00000365959.1:p.Val172Ile
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.142G>A
  hgvsp: ENSP00000473653.1:p.Val48Ile
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.418G>A
  hgvsp: ENSP00000365953.4:p.Val140Ile
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.543G>A
  hgvsp: ENST00000251547.5:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.418G>A
  hgvsp: ENSP00000389820.1:p.Val140Ile
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.543G>A
  hgvsp: ENST00000376770.1:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.418G>A
  hgvsp: ENSP00000251546.4:p.Val140Ile
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.418G>A
  hgvsp: ENSP00000365951.1:p.Val140Ile
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.189G>A
  hgvsp: ENSP00000473420.1:p.Val64Ile
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3000
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val48Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

1-11718849-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718849
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718849
    reference: chr 1
allele count: 1
allele frequency: 8.322237017310253e-6
allele num: 120160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.420C>T
  hgvsp: ENST00000376760.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.144C>T
  hgvsp: ENST00000471895.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.420C>T
  hgvsp: ENST00000425796.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.516C>T
  hgvsp: ENST00000376768.1:c.516C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.545C>T
  hgvsp: ENSP00000251547.5:p.Ser182Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.420C>T
  hgvsp: ENST00000376762.4:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.545C>T
  hgvsp: ENSP00000365961.1:p.Ser182Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.420C>T
  hgvsp: ENST00000251546.4:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.191C>T
  hgvsp: ENST00000475435.1:c.191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3000
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser182Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

1-11718853-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718853
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718853
    reference: chr 1
allele count: 6
allele frequency: 4.9965024482862e-5
allele num: 120084
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.549C>T
  hgvsp: ENST00000376770.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.195C>T
  hgvsp: ENSP00000473420.1:p.Arg66Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.148C>T
  hgvsp: ENSP00000473653.1:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.424C>T
  hgvsp: ENSP00000389820.1:p.Arg142Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.424C>T
  hgvsp: ENSP00000251546.4:p.Arg142Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.549C>T
  hgvsp: ENST00000251547.5:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.520C>T
  hgvsp: ENSP00000365959.1:p.Arg174Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.424C>T
  hgvsp: ENSP00000365951.1:p.Arg142Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.424C>T
  hgvsp: ENSP00000365953.4:p.Arg142Cys
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4198
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5072
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg50Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

1-11718854-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718854
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718854
    reference: chr 1
allele count: 3
allele frequency: 2.498542516865162e-5
allele num: 120070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.425G>A
  hgvsp: ENSP00000389820.1:p.Arg142His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.196G>A
  hgvsp: ENSP00000473420.1:p.Arg66His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.550G>A
  hgvsp: ENSP00000251547.5:p.Ala184Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.425G>A
  hgvsp: ENSP00000365953.4:p.Arg142His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.425G>A
  hgvsp: ENSP00000251546.4:p.Arg142His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.149G>A
  hgvsp: ENSP00000473653.1:p.Arg50His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.521G>A
  hgvsp: ENSP00000365959.1:p.Arg174His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.550G>A
  hgvsp: ENSP00000365961.1:p.Ala184Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.425G>A
  hgvsp: ENSP00000365951.1:p.Arg142His
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala184Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

1-11718855-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718855
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718855
    reference: chr 1
allele count: 1
allele frequency: 8.328058896032513e-6
allele num: 120076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.426C>T
  hgvsp: ENST00000376760.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.551C>T
  hgvsp: ENSP00000365961.1:p.Ala184Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.426C>T
  hgvsp: ENST00000425796.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.522C>T
  hgvsp: ENST00000376768.1:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.150C>T
  hgvsp: ENST00000471895.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.426C>T
  hgvsp: ENST00000251546.4:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.551C>T
  hgvsp: ENSP00000251547.5:p.Ala184Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.197C>T
  hgvsp: ENST00000475435.1:c.197C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.426C>T
  hgvsp: ENST00000376762.4:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala184Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ

1-11718859-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718859
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718859
    reference: chr 1
allele count: 7
allele frequency: 5.833430557175953e-5
allele num: 119998
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.430C>G
  hgvsp: ENSP00000251546.4:p.Arg144Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.201C>G
  hgvsp: ENSP00000473420.1:p.Arg68Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.430C>G
  hgvsp: ENSP00000365951.1:p.Arg144Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.430C>G
  hgvsp: ENSP00000365953.4:p.Arg144Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.430C>G
  hgvsp: ENSP00000389820.1:p.Arg144Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.526C>G
  hgvsp: ENSP00000365959.1:p.Arg176Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.555C>G
  hgvsp: ENSP00000365961.1:p.His185Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.555C>G
  hgvsp: ENSP00000251547.5:p.His185Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.154C>G
  hgvsp: ENSP00000473653.1:p.Arg52Gly
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His185Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum

1-11718859-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718859
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718859
    reference: chr 1
allele count: 555
allele frequency: 4.625077084618077e-3
allele num: 119998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.430C>T
  hgvsp: ENSP00000365953.4:p.Arg144Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.430C>T
  hgvsp: ENSP00000389820.1:p.Arg144Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.555C>T
  hgvsp: ENST00000251547.5:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.201C>T
  hgvsp: ENSP00000473420.1:p.Arg68Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.526C>T
  hgvsp: ENSP00000365959.1:p.Arg176Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.555C>T
  hgvsp: ENST00000376770.1:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.430C>T
  hgvsp: ENSP00000251546.4:p.Arg144Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.154C>T
  hgvsp: ENSP00000473653.1:p.Arg52Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.430C>T
  hgvsp: ENSP00000365951.1:p.Arg144Cys
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 9.75e1
  variant carriers: 278
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 12039
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 22780
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 12700
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9138
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg52Cys
num of homozygotes: 2
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

1-11718860-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718860
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718860
    reference: chr 1
allele count: 3
allele frequency: 2.50075022506752e-5
allele num: 119964
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.556G>A
  hgvsp: ENSP00000365961.1:p.Ala186Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.202G>A
  hgvsp: ENSP00000473420.1:p.Arg68His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.431G>A
  hgvsp: ENSP00000251546.4:p.Arg144His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.155G>A
  hgvsp: ENSP00000473653.1:p.Arg52His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.431G>A
  hgvsp: ENSP00000365953.4:p.Arg144His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.556G>A
  hgvsp: ENSP00000251547.5:p.Ala186Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.431G>A
  hgvsp: ENSP00000389820.1:p.Arg144His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.431G>A
  hgvsp: ENSP00000365951.1:p.Arg144His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.527G>A
  hgvsp: ENSP00000365959.1:p.Arg176His
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2996
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31169
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala186Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

1-11718861-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718861
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718861
    reference: chr 1
allele count: 6
allele frequency: 5.001333688983729e-5
allele num: 119968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.156C>T
  hgvsp: ENST00000471895.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.432C>T
  hgvsp: ENST00000376762.4:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.203C>T
  hgvsp: ENST00000475435.1:c.203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.432C>T
  hgvsp: ENST00000251546.4:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.432C>T
  hgvsp: ENST00000425796.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.528C>T
  hgvsp: ENST00000376768.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.432C>T
  hgvsp: ENST00000376760.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.557C>T
  hgvsp: ENSP00000365961.1:p.Ala186Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.557C>T
  hgvsp: ENSP00000251547.5:p.Ala186Val
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 9220
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4823
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3291
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala186Val
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

1-11718862-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718862
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718862
    reference: chr 1
allele count: 4
allele frequency: 3.334945223524703e-5
allele num: 119942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.204G>A
  hgvsp: ENSP00000473420.1:p.Ala69Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.433G>A
  hgvsp: ENSP00000365953.4:p.Ala145Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.529G>A
  hgvsp: ENSP00000365959.1:p.Ala177Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.433G>A
  hgvsp: ENSP00000251546.4:p.Ala145Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.433G>A
  hgvsp: ENSP00000389820.1:p.Ala145Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.558G>A
  hgvsp: ENST00000376770.1:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.433G>A
  hgvsp: ENSP00000365951.1:p.Ala145Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.558G>A
  hgvsp: ENST00000251547.5:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.157G>A
  hgvsp: ENSP00000473653.1:p.Ala53Thr
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22952
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1887
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9211
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala53Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

1-11718869-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718869
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718869
    reference: chr 1
allele count: 1
allele frequency: 8.346966712296751e-6
allele num: 119804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.440G>A
  hgvsp: ENSP00000251546.4:p.Gly147Glu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.440G>A
  hgvsp: ENSP00000365951.1:p.Gly147Glu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.536G>A
  hgvsp: ENSP00000365959.1:p.Gly179Glu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.565G>A
  hgvsp: ENSP00000251547.5:p.Gly189Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.440G>A
  hgvsp: ENSP00000389820.1:p.Gly147Glu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.565G>A
  hgvsp: ENSP00000365961.1:p.Gly189Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.440G>A
  hgvsp: ENSP00000365953.4:p.Gly147Glu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.164G>A
  hgvsp: ENSP00000473653.1:p.Gly55Glu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.211G>A
  hgvsp: ENSP00000473420.1:p.Gly71Glu
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4192
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly189Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

1-11718875-TTCCAGCCAGACCCGGCGACCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718875
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718854
    reference: chr 1
allele count: 2
allele frequency: 1.671541997492687e-5
allele num: 119650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsp: ENSP00000251546.4:p.Arg152_Ala158del
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsp: ENSP00000365951.1:p.Arg152_Ala158del
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsp: ENSP00000365953.4:p.Arg152_Ala158del
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsp: ENSP00000389820.1:p.Arg152_Ala158del
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsp: ENSP00000365961.1:p.Pro193_Gln199del
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsp: ENSP00000251547.5:p.Pro193_Gln199del
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsp: ENSP00000473653.1:p.Arg60_Ala66del
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsp: ENSP00000473420.1:p.Arg76_Ala82del
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsp: ENSP00000365959.1:p.Arg184_Ala190del
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12790
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2994
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4817
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro193_Gln199del
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: TTCCAGCCAGACCCGGCGACCA
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

1-11718878-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718878
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718878
    reference: chr 1
allele count: 3
allele frequency: 2.510376221716428e-5
allele num: 119504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.574C>T
  hgvsp: ENSP00000251547.5:p.Gln192Ter
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.173C>T
  hgvsp: ENSP00000473653.1:p.Pro58Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.449C>T
  hgvsp: ENSP00000389820.1:p.Pro150Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.545C>T
  hgvsp: ENSP00000365959.1:p.Pro182Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.449C>T
  hgvsp: ENSP00000365953.4:p.Pro150Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.220C>T
  hgvsp: ENSP00000473420.1:p.Pro74Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.574C>T
  hgvsp: ENSP00000365961.1:p.Gln192Ter
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.449C>T
  hgvsp: ENSP00000365951.1:p.Pro150Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.449C>T
  hgvsp: ENSP00000251546.4:p.Pro150Leu
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4180
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln192Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

1-11718888-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718888
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718888
    reference: chr 1
allele count: 1
allele frequency: 8.391092016715055e-6
allele num: 119174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.230C>T
  hgvsp: ENST00000475435.1:c.230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.584C>T
  hgvsp: ENSP00000251547.5:p.Pro195Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.183C>T
  hgvsp: ENST00000471895.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.459C>T
  hgvsp: ENST00000251546.4:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.459C>T
  hgvsp: ENST00000376762.4:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.584C>T
  hgvsp: ENSP00000365961.1:p.Pro195Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.459C>T
  hgvsp: ENST00000425796.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.555C>T
  hgvsp: ENST00000376768.1:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.459C>T
  hgvsp: ENST00000376760.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4812
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro195Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ

1-11718891-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718891
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718891
    reference: chr 1
allele count: 7
allele frequency: 5.87958607714017e-5
allele num: 119056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.233C>T
  hgvsp: ENST00000475435.1:c.233C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.587C>T
  hgvsp: ENSP00000365961.1:p.Ala196Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.462C>T
  hgvsp: ENST00000376762.4:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.587C>T
  hgvsp: ENSP00000251547.5:p.Ala196Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.462C>T
  hgvsp: ENST00000376760.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.462C>T
  hgvsp: ENST00000425796.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.462C>T
  hgvsp: ENST00000251546.4:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.558C>T
  hgvsp: ENST00000376768.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.186C>T
  hgvsp: ENST00000471895.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22567
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5638
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3251
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala196Val
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum

1-11718892-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718892
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718892
    reference: chr 1
allele count: 5
allele frequency: 4.201468833504193e-5
allele num: 119006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.234G>A
  hgvsp: ENSP00000473420.1:p.Asp79Asn
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.187G>A
  hgvsp: ENSP00000473653.1:p.Asp63Asn
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.588G>A
  hgvsp: ENST00000376770.1:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.588G>A
  hgvsp: ENST00000251547.5:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.559G>A
  hgvsp: ENSP00000365959.1:p.Asp187Asn
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.463G>A
  hgvsp: ENSP00000251546.4:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.463G>A
  hgvsp: ENSP00000365953.4:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.463G>A
  hgvsp: ENSP00000389820.1:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.463G>A
  hgvsp: ENSP00000365951.1:p.Asp155Asn
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4810
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp63Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

1-11718899-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718899
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718899
    reference: chr 1
allele count: 1
allele frequency: 8.417083312290625e-6
allele num: 118806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.241C>T
  hgvsp: ENSP00000473420.1:p.Pro81Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.470C>T
  hgvsp: ENSP00000365953.4:p.Pro157Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.595C>T
  hgvsp: ENSP00000365961.1:p.Gln199Ter
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.566C>T
  hgvsp: ENSP00000365959.1:p.Pro189Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.595C>T
  hgvsp: ENSP00000251547.5:p.Gln199Ter
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.194C>T
  hgvsp: ENSP00000473653.1:p.Pro65Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.470C>T
  hgvsp: ENSP00000365951.1:p.Pro157Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.470C>T
  hgvsp: ENSP00000251546.4:p.Pro157Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.470C>T
  hgvsp: ENSP00000389820.1:p.Pro157Leu
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2979
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln199Ter
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

1-11718907-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718907
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718907
    reference: chr 1
allele count: 23
allele frequency: 1.94168200314046e-4
allele num: 118454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.478G>A
  hgvsp: ENSP00000365953.4:p.Glu160Lys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.478G>A
  hgvsp: ENSP00000251546.4:p.Glu160Lys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.478G>A
  hgvsp: ENSP00000365951.1:p.Glu160Lys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.249G>A
  hgvsp: ENSP00000473420.1:p.Glu84Lys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.202G>A
  hgvsp: ENSP00000473653.1:p.Glu68Lys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.603G>A
  hgvsp: ENST00000251547.5:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.478G>A
  hgvsp: ENSP00000389820.1:p.Glu160Lys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.574G>A
  hgvsp: ENSP00000365959.1:p.Glu192Lys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.603G>A
  hgvsp: ENST00000376770.1:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22299
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11284
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9012
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu68Lys
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

1-11718907-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718907
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718907
    reference: chr 1
allele count: 1
allele frequency: 8.442095665828085e-6
allele num: 118454
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.603G>C
  hgvsp: ENSP00000365961.1:p.Lys201Asn
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.202G>C
  hgvsp: ENSP00000473653.1:p.Glu68Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.478G>C
  hgvsp: ENSP00000251546.4:p.Glu160Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.574G>C
  hgvsp: ENSP00000365959.1:p.Glu192Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.603G>C
  hgvsp: ENSP00000251547.5:p.Lys201Asn
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.478G>C
  hgvsp: ENSP00000365953.4:p.Glu160Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000389820
  ensembl transcript: ENST00000425796
  gene symbol: FBXO44
  hgvsc: ENST00000425796.1:c.478G>C
  hgvsp: ENSP00000389820.1:p.Glu160Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.478G>C
  hgvsp: ENSP00000365951.1:p.Glu160Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.249G>C
  hgvsp: ENSP00000473420.1:p.Glu84Gln
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys201Asn
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

1-11718931-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718931
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718931
    reference: chr 1
allele count: 3
allele frequency: 2.569945345828979e-5
allele num: 116734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.270+3G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.499+3G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.499+3G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.499+3G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.624+3G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.223+3G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.624+3G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.595+3G>A
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21486
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2958
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 3.25e1
  variant carriers: 0
hgvs: c.624+3G>A
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

1-11718932-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718932
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718932
    reference: chr 1
allele count: 11
allele frequency: 9.424263193968471e-5
allele num: 116720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.270+4C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.624+4C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.499+4C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.499+4C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.223+4C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.595+4C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.624+4C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.499+4C>T
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21466
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1881
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
hgvs: c.624+4C>T
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

1-11718933-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718933
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718933
    reference: chr 1
allele count: 14
allele frequency: 1.200192030724916e-4
allele num: 116648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.499+5G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.499+5G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.624+5G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.499+5G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.223+5G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.595+5G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.270+5G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.624+5G>A
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12381
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10297
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21408
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27997
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2748
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 3.25e1
  variant carriers: 0
hgvs: c.624+5G>A
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

1-11718945-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718945
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718945
    reference: chr 1
allele count: 2
allele frequency: 1.727533427771827e-5
allele num: 115772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.624+17G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.595+17G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.223+17G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.499+17G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.270+17G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.499+17G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.624+17G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.499+17G>A
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3262
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2920
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4044
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1328
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

1-11718947-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718947
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718947
    reference: chr 1
allele count: 1
allele frequency: 8.643938870064311e-6
allele num: 115688
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.624+19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.595+19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.270+19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.624+19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.499+19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.499+19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.223+19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.499+19C>G
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20468
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1866
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4756
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3330
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2904
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

1-11718948-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718948
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718948
    reference: chr 1
allele count: 4
allele frequency: 3.462783731842028e-5
allele num: 115514
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.624+20G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.499+20G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.499+20G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.499+20G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.223+20G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.595+20G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.624+20G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.270+20G>A
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20258
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4753
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3042
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8254
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3994
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

1-11718952-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718952
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718952
    reference: chr 1
allele count: 2
allele frequency: 1.73301214841516e-5
allele num: 115406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.595+24G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.499+24G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.624+24G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.624+24G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.270+24G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.499+24G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.499+24G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.223+24G>A
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1563
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3917
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

1-11718957-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718957
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718957
    reference: chr 1
allele count: 1
allele frequency: 8.684324793747287e-6
allele num: 115150
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.624+29G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.624+29G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.595+29G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.270+29G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.499+29G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.499+29G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.223+29G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.499+29G>A
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5403
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2060
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3847
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

1-11718961-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718961
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718961
    reference: chr 1
allele count: 2
allele frequency: 1.742129928050034e-5
allele num: 114802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.624+33G>C
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.624+33G>C
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.499+33G>C
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.595+33G>C
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.223+33G>C
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.499+33G>C
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.499+33G>C
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.270+33G>C
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10650
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1663
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3785
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2446
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7255
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

1-11718965-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11718965
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11718965
    reference: chr 1
allele count: 2
allele frequency: 1.74797671695013e-5
allele num: 114418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.223+37G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.595+37G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.270+37G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.499+37G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.499+37G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.624+37G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.624+37G>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.499+37G>A
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15946
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1365
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2746
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1838
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1834
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3786
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4733
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/1-11721157-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721157
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721157
    reference: chr 1
allele count: 1
allele frequency: 8.618312189740762e-6
allele num: 116032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-30C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-30C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-30C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-30C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-30C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-30C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-30C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-30C>A
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7160
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15589
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

1-11721162-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721162
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721162
    reference: chr 1
allele count: 1
allele frequency: 8.595495960116898e-6
allele num: 116340
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-25C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-25C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-25C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-25C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-25C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-25C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-25C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-25C>T
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13152
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15588
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4816
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

1-11721163-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721163
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721164
    reference: chr 1
allele count: 1
allele frequency: 8.591803419537761e-6
allele num: 116390
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-18dupC
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-18dupC
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-18dupC
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-18dupC
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-18dupC
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-18dupC
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-18dupC
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-18dupC
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15528
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3354
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

1-11721164-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721164
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721164
    reference: chr 1
allele count: 1
allele frequency: 8.586786652698828e-6
allele num: 116458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-23C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-23C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-23C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-23C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-23C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-23C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-23C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-23C>T
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1997
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7186
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4242
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

1-11721166-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721166
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721166
    reference: chr 1
allele count: 18
allele frequency: 1.541782300339192e-4
allele num: 116748
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-21C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-21C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-21C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-21C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-21C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-21C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-21C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-21C>T
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4391
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8988
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4245
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15800
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

1-11721167-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721167
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721167
    reference: chr 1
allele count: 1
allele frequency: 8.557394444539527e-6
allele num: 116858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-20C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-20C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-20C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-20C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-20C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-20C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-20C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-20C>G
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4249
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15586
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/1-11721168-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721168
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721168
    reference: chr 1
allele count: 7
allele frequency: 5.984031185351091e-5
allele num: 116978
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-19C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-19C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-19C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-19C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-19C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-19C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-19C>A
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-19C>A
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15586
  bin: 9.75e1
  variant carriers: 7
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-11721168-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721168
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721168
    reference: chr 1
allele count: 7
allele frequency: 5.984031185351091e-5
allele num: 116978
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-19C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-19C>G
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3352
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4813
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2222
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

1-11721168-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721168
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721168
    reference: chr 1
allele count: 2
allele frequency: 1.709723195814597e-5
allele num: 116978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-19C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-19C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-19C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-19C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-19C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-19C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-19C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-19C>T
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3171
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4813
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3352
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

1-11721169-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721169
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721169
    reference: chr 1
allele count: 3
allele frequency: 2.56278831368529e-5
allele num: 117060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-18C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-18C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-18C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-18C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-18C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-18C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-18C>G
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-18C>G
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3175
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4254
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4818
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum

1-11721169-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721169
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721169
    reference: chr 1
allele count: 1
allele frequency: 8.542627712284299e-6
allele num: 117060
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-18C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-18C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-18C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-18C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-18C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-18C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-18C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-18C>T
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6463
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2178
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1997
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7249
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

1-11721174-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721174
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721174
    reference: chr 1
allele count: 3
allele frequency: 2.549069589599796e-5
allele num: 117690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-13C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-13C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-13C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-13C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-13C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-13C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-13C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-13C>T
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4832
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1897
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16674
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

1-11721178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721178
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721178
    reference: chr 1
allele count: 1
allele frequency: 8.45809016324114e-6
allele num: 118230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-9C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-9C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-9C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-9C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-9C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-9C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-9C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-9C>T
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13212
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7339
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

1-11721184-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721184
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721184
    reference: chr 1
allele count: 3
allele frequency: 2.519653295706511e-5
allele num: 119064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.625-3C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.500-3C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.500-3C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.596-3C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.625-3C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.224-3C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.271-3C>T
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.500-3C>T
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7391
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3351
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4846
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
hgvs: c.625-3C>T
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

1-11721189-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721189
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721189
    reference: chr 1
allele count: 1
allele frequency: 8.363301831563101e-6
allele num: 119570
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.627C>T
  hgvsp: ENST00000376770.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.502C>T
  hgvsp: ENSP00000251546.4:p.Leu168Phe
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.273C>T
  hgvsp: ENSP00000473420.1:p.Leu92Phe
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.627C>T
  hgvsp: ENST00000251547.5:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.226C>T
  hgvsp: ENSP00000473653.1:p.Leu76Phe
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.502C>T
  hgvsp: ENSP00000365951.1:p.Leu168Phe
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.502C>T
  hgvsp: ENSP00000365953.4:p.Leu168Phe
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.598C>T
  hgvsp: ENSP00000365959.1:p.Leu200Phe
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3202
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu76Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS

1-11721204-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721204
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721204
    reference: chr 1
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.241C>T
  hgvsp: ENSP00000473653.1:p.Gln81Ter
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.517C>T
  hgvsp: ENSP00000365953.4:p.Gln173Ter
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.642C>T
  hgvsp: ENST00000251547.5:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.288C>T
  hgvsp: ENSP00000473420.1:p.Gln97Ter
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.517C>T
  hgvsp: ENSP00000365951.1:p.Gln173Ter
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.642C>T
  hgvsp: ENST00000376770.1:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.613C>T
  hgvsp: ENSP00000365959.1:p.Gln205Ter
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.517C>T
  hgvsp: ENSP00000251546.4:p.Gln173Ter
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2002
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4853
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln81Ter
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

1-11721212-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721212
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721212
    reference: chr 1
allele count: 2
allele frequency: 1.653548515113433e-5
allele num: 120952
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.650C>T
  hgvsp: ENSP00000365961.1:p.Pro217Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.525C>T
  hgvsp: ENST00000376762.4:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.525C>T
  hgvsp: ENST00000376760.1:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.296C>T
  hgvsp: ENST00000475435.1:c.296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.650C>T
  hgvsp: ENSP00000251547.5:p.Pro217Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.621C>T
  hgvsp: ENST00000376768.1:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.249C>T
  hgvsp: ENST00000471895.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.525C>T
  hgvsp: ENST00000251546.4:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19333
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro217Leu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

1-11721213-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721213
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721213
    reference: chr 1
allele count: 146
allele frequency: 1.206392226206805e-3
allele num: 121022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.622G>A
  hgvsp: ENSP00000365959.1:p.Ala208Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.250G>A
  hgvsp: ENSP00000473653.1:p.Ala84Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.651G>A
  hgvsp: ENST00000376770.1:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.526G>A
  hgvsp: ENSP00000365953.4:p.Ala176Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.297G>A
  hgvsp: ENSP00000473420.1:p.Ala100Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.526G>A
  hgvsp: ENSP00000251546.4:p.Ala176Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.526G>A
  hgvsp: ENSP00000365951.1:p.Ala176Thr
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.651G>A
  hgvsp: ENST00000251547.5:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.75e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8999
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3211
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala84Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-11721214-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721214
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721214
    reference: chr 1
allele count: 1
allele frequency: 8.262004692818665e-6
allele num: 121036
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.251C>G
  hgvsp: ENSP00000473653.1:p.Ala84Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.298C>G
  hgvsp: ENSP00000473420.1:p.Ala100Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.652C>G
  hgvsp: ENSP00000365961.1:p.Pro218Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.527C>G
  hgvsp: ENSP00000365951.1:p.Ala176Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.527C>G
  hgvsp: ENSP00000365953.4:p.Ala176Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.652C>G
  hgvsp: ENSP00000251547.5:p.Pro218Ala
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.527C>G
  hgvsp: ENSP00000251546.4:p.Ala176Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.623C>G
  hgvsp: ENSP00000365959.1:p.Ala208Gly
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4875
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro218Ala
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

1-11721216-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721216
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721216
    reference: chr 1
allele count: 4
allele frequency: 3.303710066404573e-5
allele num: 121076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.529C>T
  hgvsp: ENSP00000365951.1:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.529C>T
  hgvsp: ENSP00000251546.4:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.300C>T
  hgvsp: ENSP00000473420.1:p.Arg101Trp
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.625C>T
  hgvsp: ENSP00000365959.1:p.Arg209Trp
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.253C>T
  hgvsp: ENSP00000473653.1:p.Arg85Trp
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.529C>T
  hgvsp: ENSP00000365953.4:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.654C>T
  hgvsp: ENST00000376770.1:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.654C>T
  hgvsp: ENST00000251547.5:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15498
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4875
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg85Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

1-11721217-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721217
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721217
    reference: chr 1
allele count: 3
allele frequency: 2.477455158061639e-5
allele num: 121092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.530G>A
  hgvsp: ENSP00000251546.4:p.Arg177Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.530G>A
  hgvsp: ENSP00000365953.4:p.Arg177Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.626G>A
  hgvsp: ENSP00000365959.1:p.Arg209Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.655G>A
  hgvsp: ENSP00000251547.5:p.Gly219Ser
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.301G>A
  hgvsp: ENSP00000473420.1:p.Arg101Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.655G>A
  hgvsp: ENSP00000365961.1:p.Gly219Ser
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.530G>A
  hgvsp: ENSP00000365951.1:p.Arg177Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.254G>A
  hgvsp: ENSP00000473653.1:p.Arg85Gln
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly219Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

1-11721217-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721217
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721217
    reference: chr 1
allele count: 2
allele frequency: 1.651636772041093e-5
allele num: 121092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.530G>C
  hgvsp: ENSP00000365953.4:p.Arg177Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.530G>C
  hgvsp: ENSP00000365951.1:p.Arg177Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.655G>C
  hgvsp: ENSP00000251547.5:p.Gly219Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.254G>C
  hgvsp: ENSP00000473653.1:p.Arg85Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.626G>C
  hgvsp: ENSP00000365959.1:p.Arg209Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.530G>C
  hgvsp: ENSP00000251546.4:p.Arg177Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.301G>C
  hgvsp: ENSP00000473420.1:p.Arg101Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.655G>C
  hgvsp: ENSP00000365961.1:p.Gly219Arg
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4879
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly219Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

1-11721220-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721220
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721220
    reference: chr 1
allele count: 2
allele frequency: 1.650900566258894e-5
allele num: 121146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.629G>A
  hgvsp: ENSP00000365959.1:p.Arg210His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.533G>A
  hgvsp: ENSP00000365953.4:p.Arg178His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.533G>A
  hgvsp: ENSP00000251546.4:p.Arg178His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.658G>A
  hgvsp: ENSP00000251547.5:p.Val220Ile
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.533G>A
  hgvsp: ENSP00000365951.1:p.Arg178His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.257G>A
  hgvsp: ENSP00000473653.1:p.Arg86His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.658G>A
  hgvsp: ENSP00000365961.1:p.Val220Ile
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.304G>A
  hgvsp: ENSP00000473420.1:p.Arg102His
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19567
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val220Ile
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

1-11721223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721223
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721223
    reference: chr 1
allele count: 2
allele frequency: 1.650355651642929e-5
allele num: 121186
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.661C>T
  hgvsp: ENSP00000365961.1:p.Arg221Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.536C>T
  hgvsp: ENSP00000365953.4:p.Pro179Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.661C>T
  hgvsp: ENSP00000251547.5:p.Arg221Cys
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.632C>T
  hgvsp: ENSP00000365959.1:p.Pro211Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.260C>T
  hgvsp: ENSP00000473653.1:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.536C>T
  hgvsp: ENSP00000251546.4:p.Pro179Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.307C>T
  hgvsp: ENSP00000473420.1:p.Pro103Leu
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.536C>T
  hgvsp: ENSP00000365951.1:p.Pro179Leu
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7595
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg221Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

1-11721224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721224
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721224
    reference: chr 1
allele count: 3
allele frequency: 2.475124993812188e-5
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.537G>A
  hgvsp: ENST00000376762.4:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.662G>A
  hgvsp: ENSP00000365961.1:p.Arg221His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.662G>A
  hgvsp: ENSP00000251547.5:p.Arg221His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.537G>A
  hgvsp: ENST00000376760.1:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.537G>A
  hgvsp: ENST00000251546.4:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.633G>A
  hgvsp: ENST00000376768.1:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.261G>A
  hgvsp: ENST00000471895.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.308G>A
  hgvsp: ENST00000475435.1:c.308G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4276
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg221His
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD

1-11721226-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721226
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721226
    reference: chr 1
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.539T>C
  hgvsp: ENSP00000365953.4:p.Leu180Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.539T>C
  hgvsp: ENSP00000251546.4:p.Leu180Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.539T>C
  hgvsp: ENSP00000365951.1:p.Leu180Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.263T>C
  hgvsp: ENSP00000473653.1:p.Leu88Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.635T>C
  hgvsp: ENSP00000365959.1:p.Leu212Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.664T>C
  hgvsp: ENSP00000251547.5:p.Tyr222His
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.310T>C
  hgvsp: ENSP00000473420.1:p.Leu104Pro
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.664T>C
  hgvsp: ENSP00000365961.1:p.Tyr222His
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19644
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15489
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Tyr222His
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

1-11721229-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721229
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721229
    reference: chr 1
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.638A>G
  hgvsp: ENSP00000365959.1:p.His213Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.542A>G
  hgvsp: ENSP00000251546.4:p.His181Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.266A>G
  hgvsp: ENSP00000473653.1:p.His89Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.542A>G
  hgvsp: ENSP00000365951.1:p.His181Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.667A>G
  hgvsp: ENSP00000251547.5:p.Ile223Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.667A>G
  hgvsp: ENSP00000365961.1:p.Ile223Val
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.542A>G
  hgvsp: ENSP00000365953.4:p.His181Arg
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.313A>G
  hgvsp: ENSP00000473420.1:p.His105Arg
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7609
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4278
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4879
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile223Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

1-11721243-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721243
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721243
    reference: chr 1
allele count: 3
allele frequency: 2.473859550747106e-5
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.556C>G
  hgvsp: ENSP00000365951.1:p.Arg186Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.681C>G
  hgvsp: ENSP00000365961.1:p.His227Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.556C>G
  hgvsp: ENSP00000365953.4:p.Arg186Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.556C>G
  hgvsp: ENSP00000251546.4:p.Arg186Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.280C>G
  hgvsp: ENSP00000473653.1:p.Arg94Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.681C>G
  hgvsp: ENSP00000251547.5:p.His227Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.327C>G
  hgvsp: ENSP00000473420.1:p.Arg110Gly
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.652C>G
  hgvsp: ENSP00000365959.1:p.Arg218Gly
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7603
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His227Gln
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

1-11721244-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721244
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721244
    reference: chr 1
allele count: 4
allele frequency: 3.298479400996141e-5
allele num: 121268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.328G>A
  hgvsp: ENSP00000473420.1:p.Arg110Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.557G>A
  hgvsp: ENSP00000365951.1:p.Arg186Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.557G>A
  hgvsp: ENSP00000365953.4:p.Arg186Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.653G>A
  hgvsp: ENSP00000365959.1:p.Arg218Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.557G>A
  hgvsp: ENSP00000251546.4:p.Arg186Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.682G>A
  hgvsp: ENSP00000365961.1:p.Gly228Ser
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.682G>A
  hgvsp: ENSP00000251547.5:p.Gly228Ser
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.281G>A
  hgvsp: ENSP00000473653.1:p.Arg94Gln
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9009
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4875
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly228Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

1-11721246-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721246
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721246
    reference: chr 1
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.330C>T
  hgvsp: ENSP00000473420.1:p.Arg111Trp
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.684C>T
  hgvsp: ENST00000251547.5:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.559C>T
  hgvsp: ENSP00000365951.1:p.Arg187Trp
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.684C>T
  hgvsp: ENST00000376770.1:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.559C>T
  hgvsp: ENSP00000251546.4:p.Arg187Trp
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.559C>T
  hgvsp: ENSP00000365953.4:p.Arg187Trp
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.655C>T
  hgvsp: ENSP00000365959.1:p.Arg219Trp
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.283C>T
  hgvsp: ENSP00000473653.1:p.Arg95Trp
  variant of: http://identifiers.org/hgnc/24847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5673
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4875
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg95Trp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

1-11721247-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11721247
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 11721247
    reference: chr 1
allele count: 3
allele frequency: 2.474145182839329e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473420
  ensembl transcript: ENST00000475435
  gene symbol: FBXO44
  hgvsc: ENST00000475435.1:c.331G>A
  hgvsp: ENSP00000473420.1:p.Arg111Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365961
  ensembl transcript: ENST00000376770
  gene symbol: FBXO44
  hgvsc: ENST00000376770.1:c.685G>A
  hgvsp: ENSP00000365961.1:p.Gly229Ser
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000473653
  ensembl transcript: ENST00000471895
  gene symbol: FBXO44
  hgvsc: ENST00000471895.1:c.284G>A
  hgvsp: ENSP00000473653.1:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365959
  ensembl transcript: ENST00000376768
  gene symbol: FBXO44
  hgvsc: ENST00000376768.1:c.656G>A
  hgvsp: ENSP00000365959.1:p.Arg219Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251546
  ensembl transcript: ENST00000251546
  gene symbol: FBXO44
  hgvsc: ENST00000251546.4:c.560G>A
  hgvsp: ENSP00000251546.4:p.Arg187Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000251547
  ensembl transcript: ENST00000251547
  gene symbol: FBXO44
  hgvsc: ENST00000251547.5:c.685G>A
  hgvsp: ENSP00000251547.5:p.Gly229Ser
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365953
  ensembl transcript: ENST00000376762
  gene symbol: FBXO44
  hgvsc: ENST00000376762.4:c.560G>A
  hgvsp: ENSP00000365953.4:p.Arg187Gln
  variant of: http://identifiers.org/hgnc/24847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000132879
  ensembl protein: ENSP00000365951
  ensembl transcript: ENST00000376760
  gene symbol: FBXO44
  hgvsc: ENST00000376760.1:c.560G>A
  hgvsp: ENSP00000365951.1:p.Arg187Gln
  variant of: http://identifiers.org/hgnc/24847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3214
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4274
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7600
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly229Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

1-11721249-C-T
type: Variant
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: T
canonical: false
consequence: missense
filter: PASS
hgvs: p.Arg96Cys
num of homozygotes: 0
reference allele: C

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

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

GenotypeQuality
all individuals: 5088
bin: 9.75e1
variant carriers: 3

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

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

GenotypeQuality
all individuals: 549
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3307
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3000
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31799
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9242
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.547521600727603e-5
allele num: 65970
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

FS
type: SiteQuality
SIO_000300: 1.115e0

DP
type: SiteQuality
SIO_000300: 1.804078e6

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

MQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

QD
type: SiteQuality
SIO_000300: 1.196e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-2

GenotypeQuality
all individuals: 5087
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 546
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3306
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1902
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31808
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515518913676043e-5
allele num: 65984
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.646e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e0

FS
type: SiteQuality
SIO_000300: 6.892e0

VQSLOD
type: SiteQuality
SIO_000300: -2.759e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

DP
type: SiteQuality
SIO_000300: 1.804068e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.293e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
all individuals: 31778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4204
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5087
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2999
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65984
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 9.419999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.96e-1

FS
type: SiteQuality
SIO_000300: 2.143e0

MQRankSum
type: SiteQuality
SIO_000300: -4.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-2

MQ
type: SiteQuality
SIO_000300: 5.957e1

DP
type: SiteQuality
SIO_000300: 1.804136e6

QD
type: SiteQuality
SIO_000300: 1.146e1

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 534
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3303
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4205
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31787
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5087
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9239
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.19e-1

FS
type: SiteQuality
SIO_000300: 2.26e0

DP
type: SiteQuality
SIO_000300: 1.804066e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.94e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.384e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.325e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 1347
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2997
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 559
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31772
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3301
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9241
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.946661475569399e-4
allele num: 10274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65988
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.804127e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

FS
type: SiteQuality
SIO_000300: 1.165e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.07e0

QD
type: SiteQuality
SIO_000300: 1.146e1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

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

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1902
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3301
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2996
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9240
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 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: 1
allele frequency: 1.515427047341941e-5
allele num: 65988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
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: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.212415130940834e-4
allele num: 16496
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.21e-1

DP
type: SiteQuality
SIO_000300: 1.804138e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.089e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.704e0

MQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
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SIO_000300: 1.263e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

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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bin: 3.75e1
variant carriers: 0

East Asian
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allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65980
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e0

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

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

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.546832373446499e-4
allele num: 6598
num of homozygotes: 1

European (Non-Finnish)
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allele count: 23
allele frequency: 3.487384764677341e-4
allele num: 65952
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73460537727667e-4
allele num: 11530
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.947040498442368e-4
allele num: 10272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

QD
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SIO_000300: 1.364e1

ClippingRankSum
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SIO_000300: -6.0e-1

DP
type: SiteQuality
SIO_000300: 1.805806e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.69e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.82e-1

FS
type: SiteQuality
SIO_000300: 5.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.0e-3

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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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.517680983457277e-5
allele num: 65890
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.601005722212589e-4
allele num: 11534
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.94e-1

DP
type: SiteQuality
SIO_000300: 1.801738e6

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

FS
type: SiteQuality
SIO_000300: 4.067e0

MQRankSum
type: SiteQuality
SIO_000300: -6.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.57e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.176e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -9.12e-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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variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65888
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.601005722212589e-4
allele num: 11534
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.377e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.269e1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.801785e6

FS
type: SiteQuality
SIO_000300: 5.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16502
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.518602885345482e-5
allele num: 65850
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.75800156128025e-5
allele num: 10248
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Other
type: Population
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allele frequency: 0.0e0
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Latino
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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MQ
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DP
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QD
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
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allele num: 11534
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.519295047098146e-5
allele num: 65820
num of homozygotes: 0

South Asian
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InbreedingCoeff
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MQ
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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DP
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FS
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VQSLOD
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 4
allele frequency: 6.082725060827251e-5
allele num: 65760
num of homozygotes: 0

African
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
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FS
type: SiteQuality
SIO_000300: 1.741e0

InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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VQSLOD
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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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South Asian
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allele count: 3
allele frequency: 1.817961459217065e-4
allele num: 16502
num of homozygotes: 0

European (Finnish)
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allele num: 6586
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African
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Other
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European (Non-Finnish)
type: Population
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allele frequency: 0.0e0
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East Asian
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Latino
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QD
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 2.842e0

MQRankSum
type: SiteQuality
SIO_000300: 5.89e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e-1

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4197
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
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GenotypeQuality
all individuals: 31232
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5066
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3291
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.790483649892304e-5
allele num: 10214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65754
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.95e-1

DP
type: SiteQuality
SIO_000300: 1.797193e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

QD
type: SiteQuality
SIO_000300: 1.129e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 908
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
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GenotypeQuality
all individuals: 2968
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4158
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31007
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 37
bin: 5.75e1
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GenotypeQuality
all individuals: 1327
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 23
bin: 1.25e1
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GenotypeQuality
all individuals: 5327
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.065384147083891e-4
allele num: 65704
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.69e-1

DP
type: SiteQuality
SIO_000300: 1.825244e6

QD
type: SiteQuality
SIO_000300: 1.249e1

FS
type: SiteQuality
SIO_000300: 1.105e0

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
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variant carriers: 1

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3262
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 4158
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variant carriers: 0

GenotypeQuality
all individuals: 5327
bin: 9.75e1
variant carriers: 553

GenotypeQuality
all individuals: 111
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31007
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2968
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1327
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.073489219556636e-4
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 30
allele frequency: 2.942907592701589e-3
allele num: 10194
num of homozygotes: 0

Latino
type: Population
allele count: 97
allele frequency: 8.409918501820704e-3
allele num: 11534
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 7.878787878787879e-4
allele num: 16500
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.567928730512249e-3
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 405
allele frequency: 6.1640082795568e-3
allele num: 65704
num of homozygotes: 2

East Asian
type: Population
allele count: 1
allele frequency: 1.165229550221394e-4
allele num: 8582
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.72e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

DP
type: SiteQuality
SIO_000300: 1.825244e6

FS
type: SiteQuality
SIO_000300: 1.105e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 1.249e1

GenotypeQuality
all individuals: 130
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 9223
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variant carriers: 0

GenotypeQuality
all individuals: 126
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GenotypeQuality
all individuals: 4201
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GenotypeQuality
all individuals: 4822
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variant carriers: 3

GenotypeQuality
all individuals: 1345
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GenotypeQuality
all individuals: 140
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GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 930
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variant carriers: 0

GenotypeQuality
all individuals: 3292
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522579859313621e-5
allele num: 65678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73460537727667e-4
allele num: 11530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

MQ
type: SiteQuality
SIO_000300: 5.987e1

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.588e0

QD
type: SiteQuality
SIO_000300: 1.22e1

FS
type: SiteQuality
SIO_000300: 1.773e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 1.788763e6

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31262
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variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 933
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variant carriers: 0

GenotypeQuality
all individuals: 130
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variant carriers: 0

GenotypeQuality
all individuals: 4201
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GenotypeQuality
all individuals: 90
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GenotypeQuality
all individuals: 1886
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 2996
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GenotypeQuality
all individuals: 127
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GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 1345
bin: 8.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.044788843893676e-5
allele num: 65686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.927729772191673e-4
allele num: 10184
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.788917e6

FS
type: SiteQuality
SIO_000300: 1.094e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.154e0

QD
type: SiteQuality
SIO_000300: 1.306e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: -5.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeQuality
all individuals: 3289
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1345
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 2.25e1
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GenotypeQuality
all individuals: 4200
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
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GenotypeQuality
all individuals: 4820
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
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GenotypeQuality
all individuals: 93
bin: 7.5e0
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GenotypeQuality
all individuals: 10
bin: 2.5e0
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GenotypeQuality
all individuals: 129
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
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GenotypeQuality
all individuals: 2995
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31219
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.568852608814839e-5
allele num: 65662
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.03e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 1.083e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e-1

DP
type: SiteQuality
SIO_000300: 1.788042e6

FS
type: SiteQuality
SIO_000300: 2.208e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 9202
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
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GenotypeQuality
all individuals: 3288
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 142
bin: 2.75e1
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GenotypeQuality
all individuals: 98
bin: 3.75e1
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GenotypeQuality
all individuals: 1888
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variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
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GenotypeQuality
all individuals: 136
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GenotypeQuality
all individuals: 2992
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 4815
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 31155
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524715640533041e-5
allele num: 65586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10150
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.785302e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 6.79e-1

QD
type: SiteQuality
SIO_000300: 1.318e1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 5.752e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.549e0

GenotypeQuality
all individuals: 1170
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3283
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31040
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
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GenotypeQuality
all individuals: 9174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1345
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.213297743266198e-4
allele num: 16484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65492
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.441e0

FS
type: SiteQuality
SIO_000300: 2.171e0

QD
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.58e-1

MQ
type: SiteQuality
SIO_000300: 5.537e1

VQSLOD
type: SiteQuality
SIO_000300: -2.189e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

DP
type: SiteQuality
SIO_000300: 1.782761e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.54e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
allele num: 11498
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: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10090
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.820830298616169e-4
allele num: 16476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65418
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.779942e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.947e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.78e-1

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -4.199e0

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.179999999999999e-1

QD
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SIO_000300: 1.066e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533083951677194e-5
allele num: 65228
num of homozygotes: 0

East Asian
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allele count: 0
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 1.822e0

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

DP
type: SiteQuality
SIO_000300: 1.773871e6

QD
type: SiteQuality
SIO_000300: 2.541e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 888
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African
type: Population
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South Asian
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allele frequency: 6.080505898090721e-5
allele num: 16446
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 2
allele frequency: 2.345215759849906e-4
allele num: 8528
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European (Non-Finnish)
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allele count: 4
allele frequency: 6.136663496057194e-5
allele num: 65182
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
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QD
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VQSLOD
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FS
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ClippingRankSum
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MQ
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DP
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MQRankSum
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SIO_000300: -2.53e-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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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.534919416730622e-5
allele num: 65150
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.002807862013638e-4
allele num: 9972
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.520300398967379e-4
allele num: 8522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.872e0

MQRankSum
type: SiteQuality
SIO_000300: -5.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.68e-1

DP
type: SiteQuality
SIO_000300: 1.771408e6

QD
type: SiteQuality
SIO_000300: 1.146e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6526
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Other
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

African
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allele count: 1
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allele num: 9948
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -3.071e-1

InbreedingCoeff
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.926e1

MQRankSum
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.07e-1

DP
type: SiteQuality
SIO_000300: 1.767872e6

ReadPosRankSum
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SIO_000300: 1.49e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

South Asian
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European (Finnish)
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allele num: 6510
num of homozygotes: 0

Latino
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East Asian
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European (Non-Finnish)
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allele count: 21
allele frequency: 3.241741278172275e-4
allele num: 64780
num of homozygotes: 0

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

Latino
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allele frequency: 8.716875871687587e-5
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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num of homozygotes: 0

Other
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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FS
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QD
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ClippingRankSum
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele num: 16356
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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Latino
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Other
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QD
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DP
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8726
bin: 6.75e1
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GenotypeQuality
all individuals: 579
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.049758555532228e-3
allele num: 9526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56852903347241e-5
allele num: 63754
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.395e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

DP
type: SiteQuality
SIO_000300: 1.729975e6

MQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

FS
type: SiteQuality
SIO_000300: 3.232e0

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 8
allele frequency: 8.410428931875525e-4
allele num: 9512
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.116956202593589e-5
allele num: 16348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.709428275407365e-5
allele num: 63702
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.750393838613688e-4
allele num: 11426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

FS
type: SiteQuality
SIO_000300: 6.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.099e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.67e0

DP
type: SiteQuality
SIO_000300: 1.726777e6

QD
type: SiteQuality
SIO_000300: 1.384e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.165558721114277e-5
allele num: 63180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.117e1

FS
type: SiteQuality
SIO_000300: 1.743e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 1.696034e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 63136
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.790436005625879e-5
allele num: 11376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 8.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e-1

DP
type: SiteQuality
SIO_000300: 1.695312e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

FS
type: SiteQuality
SIO_000300: 2.235e0

QD
type: SiteQuality
SIO_000300: 1.388e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 287
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.173394262503174e-5
allele num: 63024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6314
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8364
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.139952921035737e-4
allele num: 9346
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.11e0

FS
type: SiteQuality
SIO_000300: 1.1357e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.21e-1

DP
type: SiteQuality
SIO_000300: 1.68857e6

QD
type: SiteQuality
SIO_000300: 1.308e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.13e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 382
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.143622722400857e-4
allele num: 9330
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62952
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16244
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.833e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

DP
type: SiteQuality
SIO_000300: 1.672709e6

QD
type: SiteQuality
SIO_000300: 1.432e1

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
all individuals: 1305
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11344
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.592508838424053e-5
allele num: 62794
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.362e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.648708e6

VQSLOD
type: SiteQuality
SIO_000300: -2.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.568e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.196726552010741e-5
allele num: 62564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.894e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.57e-1

DP
type: SiteQuality
SIO_000300: 1.617898e6

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

Latino
type: Population
allele count: 1
allele frequency: 8.847991505928154e-5
allele num: 11302
num of homozygotes: 0

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

African
type: Population
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allele frequency: 1.087429317094389e-4
allele num: 9196
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62352
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.39e-1

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 3.009e0

DP
type: SiteQuality
SIO_000300: 1.593126e6

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -8.3e-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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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4812
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3356
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65238
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12840
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.171356e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.288e0

VQSLOD
type: SiteQuality
SIO_000300: 3.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

FS
type: SiteQuality
SIO_000300: 7.25e0

QD
type: SiteQuality
SIO_000300: 1.307e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

GenotypeQuality
all individuals: 599
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4245
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7175
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15459
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3164
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2377
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.672241829062452e-5
allele num: 13034
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.029999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

DP
type: SiteQuality
SIO_000300: 2.175679e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.247e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 3.153e0

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.48e-1

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4243
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4809
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15584
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2358
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7169
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.676795045480937e-5
allele num: 10334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65324
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -9.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.25e-1

FS
type: SiteQuality
SIO_000300: 1.492e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.899e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

QD
type: SiteQuality
SIO_000300: 8.0e0

DP
type: SiteQuality
SIO_000300: 2.177164e6

GenotypeQuality
all individuals: 92
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3353
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15542
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4811
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15586
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530643482520051e-5
allele num: 65332
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.38e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.084e0

FS
type: SiteQuality
SIO_000300: 3.121e0

MQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

DP
type: SiteQuality
SIO_000300: 2.17816e6

VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

GenotypeQuality
all individuals: 571
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4815
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3164
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7227
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15587
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 3353
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 17
allele frequency: 1.645055157731759e-3
allele num: 10334
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.667013347200555e-5
allele num: 11538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65448
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13318
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 6.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

QD
type: SiteQuality
SIO_000300: 1.181e1

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.412e0

DP
type: SiteQuality
SIO_000300: 2.180928e6

GenotypeQuality
all individuals: 15913
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3172
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7238
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4815
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3354
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527183872938302e-5
allele num: 65480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13394
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.979e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 1.219e1

VQSLOD
type: SiteQuality
SIO_000300: -1.758e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 9.67e0

DP
type: SiteQuality
SIO_000300: 2.181938e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3352
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3171
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4813
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15939
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526670941345302e-5
allele num: 65502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.934610176049526e-4
allele num: 10338
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.733102253032929e-4
allele num: 11540
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.484119916889285e-4
allele num: 13476
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

QD
type: SiteQuality
SIO_000300: 1.072e1

DP
type: SiteQuality
SIO_000300: 2.18364e6

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 3.785e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.192e0

GenotypeQuality
all individuals: 50
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3171
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15939
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7248
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15586
bin: 9.75e1
variant carriers: 7

Latino
type: Population
allele count: 4
allele frequency: 3.466204506065858e-4
allele num: 11540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.420599584446424e-5
allele num: 13476
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526670941345302e-5
allele num: 65502
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 2.18364e6

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

FS
type: SiteQuality
SIO_000300: 3.785e0

QD
type: SiteQuality
SIO_000300: 1.072e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.192e0

GenotypeQuality
all individuals: 2222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15586
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 2.75e1
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GenotypeQuality
all individuals: 314
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15939
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65502
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.934610176049526e-4
allele num: 10338
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.072e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.192e0

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

FS
type: SiteQuality
SIO_000300: 3.785e0

DP
type: SiteQuality
SIO_000300: 2.18364e6

GenotypeQuality
all individuals: 16085
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3353
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15575
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7249
bin: 6.75e1
variant carriers: 0

Latino
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
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65518
num of homozygotes: 0

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

South Asian
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allele count: 3
allele frequency: 2.215330084182543e-4
allele num: 13542
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.18442e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 1.1491e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.7e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
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allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65518
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.18442e6

VQSLOD
type: SiteQuality
SIO_000300: -1.469e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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SIO_000300: 1.1491e1

ClippingRankSum
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SIO_000300: -1.47e-1

QD
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SIO_000300: 1.019e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.7e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.568574300246703e-5
allele num: 65666
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13994
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.28e-1

DP
type: SiteQuality
SIO_000300: 2.192933e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.701e0

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

QD
type: SiteQuality
SIO_000300: 1.242e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.950236308034473e-5
allele num: 14388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.200304e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.467e0

MQRankSum
type: SiteQuality
SIO_000300: 5.07e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: -4.55e-1

GenotypeQuality
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bin: 8.75e1
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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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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variant carriers: 3

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14958
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.542426261280358e-5
allele num: 66044
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.523e0

DP
type: SiteQuality
SIO_000300: 2.209818e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.208e0

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.11e-1

QD
type: SiteQuality
SIO_000300: 1.233e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 880
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66186
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-2

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.234e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.828e1

FS
type: SiteQuality
SIO_000300: 5.468e0

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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bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16030
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505615947484116e-5
allele num: 66418
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.577e0

BaseQRankSum
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SIO_000300: -6.372e0

VQSLOD
type: SiteQuality
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MQ
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SIO_000300: 5.99e1

ReadPosRankSum
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ClippingRankSum
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QD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.228562e6

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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variant carriers: 0

African
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allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
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allele count: 0
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allele num: 16302
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.11e-1

ReadPosRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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SIO_000300: 0.0e0

FS
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MQ
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VQSLOD
type: SiteQuality
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ClippingRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 139
allele frequency: 1.337052712581762e-2
allele num: 10396
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

Latino
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allele count: 6
allele frequency: 5.186721991701245e-4
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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QD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 18
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3215
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502990951994469e-5
allele num: 66534
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

MQRankSum
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SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.082e0

DP
type: SiteQuality
SIO_000300: 2.232228e6

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

FS
type: SiteQuality
SIO_000300: 1.103e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.071e1

MQ
type: SiteQuality
SIO_000300: 5.887e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.508837321149453e-5
allele num: 66536
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.233169e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 5.921e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.57e-1

FS
type: SiteQuality
SIO_000300: 5.2e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 194
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502629601803156e-5
allele num: 66550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.61e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 2.233334e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

FS
type: SiteQuality
SIO_000300: 3.233e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.03e-1

QD
type: SiteQuality
SIO_000300: 1.145e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3218
bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502629601803156e-5
allele num: 66550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.61e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 3.233e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.145e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.233334e6

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

GenotypeQuality
all individuals: 1
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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: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502223290469895e-5
allele num: 66568
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.23e-1

DP
type: SiteQuality
SIO_000300: 2.23362e6

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

FS
type: SiteQuality
SIO_000300: 1.097e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.296e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4873
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3220
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variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.923076923076923e-4
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 2.234132e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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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
all individuals: 19605
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501726986033939e-5
allele num: 66590
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 4.064e0

DP
type: SiteQuality
SIO_000300: 2.234289e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.359e1

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 7611
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

East Asian
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -9.28e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.787e0

QD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 19642
bin: 6.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.18e-1

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.247e0

FS
type: SiteQuality
SIO_000300: 7.3e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.18e1

VQSLOD
type: SiteQuality
SIO_000300: 3.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e0

DP
type: SiteQuality
SIO_000300: 2.23438e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 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
allele num: 16506
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002011347602894e-5
allele num: 66622
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

QD
type: SiteQuality
SIO_000300: 1.041e1

FS
type: SiteQuality
SIO_000300: 1.783e0

VQSLOD
type: SiteQuality
SIO_000300: 8.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.68e-1

DP
type: SiteQuality
SIO_000300: 2.233954e6

MQ
type: SiteQuality
SIO_000300: 5.901e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele frequency: 3.002011347602894e-5
allele num: 66622
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.377e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
type: SiteQuality
SIO_000300: 1.519e1

FS
type: SiteQuality
SIO_000300: 5.966e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.233953e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

Other
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allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 2.233726e6

VQSLOD
type: SiteQuality
SIO_000300: 4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.962e0

QD
type: SiteQuality
SIO_000300: 1.008e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66608
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Latino
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allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 4.952e0

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.25e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.233815e6

ReadPosRankSum
type: SiteQuality
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MQ
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InbreedingCoeff
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VQSLOD
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QD
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