8-11696027-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696027
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696027
    reference: chr 8
allele count: 1
allele frequency: 8.343902276216541e-6
allele num: 119848
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.971C>G
  hgvsp: ENSP00000432331.1:p.Ser324Trp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.908C>G
  hgvsp: ENSP00000436069.1:p.Ser303Trp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.971C>G
  hgvsp: ENSP00000431749.1:p.Ser324Trp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1034C>G
  hgvsp: ENSP00000390367.2:p.Ser345Trp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.866C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1222C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1441C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1142C>G
  hgvsp: ENSP00000434714.1:p.Ser381Trp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.908C>G
  hgvsp: ENSP00000431649.1:p.Ser303Trp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.830C>G
  hgvsp: ENSP00000444248.1:p.Ser277Trp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1163C>G
  hgvsp: ENSP00000220584.4:p.Ser388Trp
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser388Trp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

8-11696028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696028
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696028
    reference: chr 8
allele count: 1
allele frequency: 8.339727124128499e-6
allele num: 119908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.909G>A
  hgvsp: ENST00000525777.1:c.909G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1223G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1035G>A
  hgvsp: ENST00000443614.2:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.831G>A
  hgvsp: ENST00000538689.1:c.831G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1164G>A
  hgvsp: ENST00000220584.4:c.1164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1143G>A
  hgvsp: ENST00000525900.1:c.1143G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.867G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1442G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.909G>A
  hgvsp: ENST00000528643.1:c.909G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.972G>A
  hgvsp: ENST00000530664.1:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.972G>A
  hgvsp: ENST00000528812.1:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser388Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

8-11696031-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696031
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696031
    reference: chr 8
allele count: 1
allele frequency: 8.333750020834376e-6
allele num: 119994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1445T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1038T>C
  hgvsp: ENST00000443614.2:c.1038T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.975T>C
  hgvsp: ENST00000528812.1:c.975T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.912T>C
  hgvsp: ENST00000525777.1:c.912T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.975T>C
  hgvsp: ENST00000530664.1:c.975T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1226T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.834T>C
  hgvsp: ENST00000538689.1:c.834T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1167T>C
  hgvsp: ENST00000220584.4:c.1167T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.870T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.912T>C
  hgvsp: ENST00000528643.1:c.912T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1146T>C
  hgvsp: ENST00000525900.1:c.1146T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe389Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

8-11696031-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696031
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696031
    reference: chr 8
allele count: 3
allele frequency: 2.500125006250312e-5
allele num: 119994
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1167T>G
  hgvsp: ENSP00000220584.4:p.Phe389Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1445T>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.975T>G
  hgvsp: ENSP00000432331.1:p.Phe325Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.834T>G
  hgvsp: ENSP00000444248.1:p.Phe278Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1146T>G
  hgvsp: ENSP00000434714.1:p.Phe382Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.912T>G
  hgvsp: ENSP00000431649.1:p.Phe304Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.912T>G
  hgvsp: ENSP00000436069.1:p.Phe304Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1226T>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.975T>G
  hgvsp: ENSP00000431749.1:p.Phe325Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1038T>G
  hgvsp: ENSP00000390367.2:p.Phe346Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.870T>G
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16153
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe389Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

8-11696032-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696032
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696032
    reference: chr 8
allele count: 1
allele frequency: 8.336112037345782e-6
allele num: 119960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.835G>A
  hgvsp: ENSP00000444248.1:p.Val279Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1147G>A
  hgvsp: ENSP00000434714.1:p.Val383Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1227G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.913G>A
  hgvsp: ENSP00000436069.1:p.Val305Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1446G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1039G>A
  hgvsp: ENSP00000390367.2:p.Val347Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.871G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.976G>A
  hgvsp: ENSP00000432331.1:p.Val326Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.976G>A
  hgvsp: ENSP00000431749.1:p.Val326Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.913G>A
  hgvsp: ENSP00000431649.1:p.Val305Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1168G>A
  hgvsp: ENSP00000220584.4:p.Val390Ile
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val390Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

8-11696032-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696032
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696032
    reference: chr 8
allele count: 1
allele frequency: 8.336112037345782e-6
allele num: 119960
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.976G>C
  hgvsp: ENSP00000432331.1:p.Val326Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1227G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.835G>C
  hgvsp: ENSP00000444248.1:p.Val279Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1446G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.913G>C
  hgvsp: ENSP00000431649.1:p.Val305Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.913G>C
  hgvsp: ENSP00000436069.1:p.Val305Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1147G>C
  hgvsp: ENSP00000434714.1:p.Val383Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.976G>C
  hgvsp: ENSP00000431749.1:p.Val326Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1168G>C
  hgvsp: ENSP00000220584.4:p.Val390Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.871G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1039G>C
  hgvsp: ENSP00000390367.2:p.Val347Leu
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val390Leu
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-11696035-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696035
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696035
    reference: chr 8
allele count: 1
allele frequency: 8.330417687142833e-6
allele num: 120042
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.979A>G
  hgvsp: ENSP00000432331.1:p.Met327Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1042A>G
  hgvsp: ENSP00000390367.2:p.Met348Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1171A>G
  hgvsp: ENSP00000220584.4:p.Met391Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.874A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.916A>G
  hgvsp: ENSP00000431649.1:p.Met306Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.979A>G
  hgvsp: ENSP00000431749.1:p.Met327Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.916A>G
  hgvsp: ENSP00000436069.1:p.Met306Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1230A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1150A>G
  hgvsp: ENSP00000434714.1:p.Met384Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.838A>G
  hgvsp: ENSP00000444248.1:p.Met280Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1449A>G
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met391Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-11696045-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696045
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696045
    reference: chr 8
allele count: 1
allele frequency: 8.327642777435419e-6
allele num: 120082
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.848C>A
  hgvsp: ENSP00000444248.1:p.Ala283Asp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.989C>A
  hgvsp: ENSP00000432331.1:p.Ala330Asp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.989C>A
  hgvsp: ENSP00000431749.1:p.Ala330Asp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1181C>A
  hgvsp: ENSP00000220584.4:p.Ala394Asp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1160C>A
  hgvsp: ENSP00000434714.1:p.Ala387Asp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.926C>A
  hgvsp: ENSP00000436069.1:p.Ala309Asp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1052C>A
  hgvsp: ENSP00000390367.2:p.Ala351Asp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1459C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.926C>A
  hgvsp: ENSP00000431649.1:p.Ala309Asp
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.884C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1240C>A
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16497
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala394Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

8-11696050-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696050
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696050
    reference: chr 8
allele count: 1
allele frequency: 8.310617645103384e-6
allele num: 120328
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1186C>G
  hgvsp: ENSP00000220584.4:p.Leu396Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.994C>G
  hgvsp: ENSP00000432331.1:p.Leu332Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1165C>G
  hgvsp: ENSP00000434714.1:p.Leu389Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.931C>G
  hgvsp: ENSP00000436069.1:p.Leu311Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1245C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.994C>G
  hgvsp: ENSP00000431749.1:p.Leu332Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.889C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.853C>G
  hgvsp: ENSP00000444248.1:p.Leu285Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1057C>G
  hgvsp: ENSP00000390367.2:p.Leu353Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.931C>G
  hgvsp: ENSP00000431649.1:p.Leu311Val
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1464C>G
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu396Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

8-11696055-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696055
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696055
    reference: chr 8
allele count: 4
allele frequency: 3.32016335203692e-5
allele num: 120476
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1191C>T
  hgvsp: ENST00000220584.4:c.1191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1170C>T
  hgvsp: ENST00000525900.1:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1250C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1469C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.936C>T
  hgvsp: ENST00000528643.1:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.894C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.936C>T
  hgvsp: ENST00000525777.1:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.858C>T
  hgvsp: ENST00000538689.1:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1062C>T
  hgvsp: ENST00000443614.2:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.999C>T
  hgvsp: ENST00000528812.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.999C>T
  hgvsp: ENST00000530664.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12088
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22151
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser397Ser
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

8-11696057-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696057
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696057
    reference: chr 8
allele count: 1
allele frequency: 8.294487483618387e-6
allele num: 120562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1471G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.896G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1252G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1193G>T
  hgvsp: ENSP00000220584.4:p.Trp398Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1064G>T
  hgvsp: ENSP00000390367.2:p.Trp355Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.938G>T
  hgvsp: ENSP00000436069.1:p.Trp313Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.938G>T
  hgvsp: ENSP00000431649.1:p.Trp313Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1172G>T
  hgvsp: ENSP00000434714.1:p.Trp391Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1001G>T
  hgvsp: ENSP00000431749.1:p.Trp334Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.860G>T
  hgvsp: ENSP00000444248.1:p.Trp287Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1001G>T
  hgvsp: ENSP00000432331.1:p.Trp334Leu
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp398Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

8-11696061-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696061
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696061
    reference: chr 8
allele count: 231
allele frequency: 1.91402624950285e-3
allele num: 120688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.900G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.864G>A
  hgvsp: ENST00000538689.1:c.864G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1005G>A
  hgvsp: ENST00000530664.1:c.1005G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1197G>A
  hgvsp: ENST00000220584.4:c.1197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1475G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.942G>A
  hgvsp: ENST00000525777.1:c.942G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1176G>A
  hgvsp: ENST00000525900.1:c.1176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1005G>A
  hgvsp: ENST00000528812.1:c.1005G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1068G>A
  hgvsp: ENST00000443614.2:c.1068G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.942G>A
  hgvsp: ENST00000528643.1:c.942G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1256G>A
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12124
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 17067
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 22257
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
hgvs: p.Gln399Gln
num of homozygotes: 3
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-11696069-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696069
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696069
    reference: chr 8
allele count: 2
allele frequency: 1.655026314918407e-5
allele num: 120844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1013C>T
  hgvsp: ENSP00000432331.1:p.Thr338Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1013C>T
  hgvsp: ENSP00000431749.1:p.Thr338Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.950C>T
  hgvsp: ENSP00000436069.1:p.Thr317Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1184C>T
  hgvsp: ENSP00000434714.1:p.Thr395Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.872C>T
  hgvsp: ENSP00000444248.1:p.Thr291Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.908C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1205C>T
  hgvsp: ENSP00000220584.4:p.Thr402Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.950C>T
  hgvsp: ENSP00000431649.1:p.Thr317Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1483C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1076C>T
  hgvsp: ENSP00000390367.2:p.Thr359Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1264C>T
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr402Ile
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

8-11696071-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696071
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696071
    reference: chr 8
allele count: 1
allele frequency: 8.270067318347971e-6
allele num: 120918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1015A>T
  hgvsp: ENSP00000432331.1:p.Thr339Ser
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1186A>T
  hgvsp: ENSP00000434714.1:p.Thr396Ser
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1485A>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.952A>T
  hgvsp: ENSP00000436069.1:p.Thr318Ser
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.952A>T
  hgvsp: ENSP00000431649.1:p.Thr318Ser
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1266A>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1207A>T
  hgvsp: ENSP00000220584.4:p.Thr403Ser
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1015A>T
  hgvsp: ENSP00000431749.1:p.Thr339Ser
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1078A>T
  hgvsp: ENSP00000390367.2:p.Thr360Ser
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.910A>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.874A>T
  hgvsp: ENSP00000444248.1:p.Thr292Ser
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr403Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum

8-11696073-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696073
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696073
    reference: chr 8
allele count: 1
allele frequency: 8.267879288962381e-6
allele num: 120950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.954T>A
  hgvsp: ENST00000528643.1:c.954T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.912T>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1487T>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1268T>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1017T>A
  hgvsp: ENST00000530664.1:c.1017T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1017T>A
  hgvsp: ENST00000528812.1:c.1017T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1209T>A
  hgvsp: ENST00000220584.4:c.1209T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.954T>A
  hgvsp: ENST00000525777.1:c.954T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1080T>A
  hgvsp: ENST00000443614.2:c.1080T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.876T>A
  hgvsp: ENST00000538689.1:c.876T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1188T>A
  hgvsp: ENST00000525900.1:c.1188T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr403Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

8-11696075-T-TCAGGTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696075
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696081
    reference: chr 8
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: TCAGGTA
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1191_1192insAGGTAC
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1490_1491insAGGTAC
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.957_958insAGGTAC
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1020_1021insAGGTAC
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.915_916insAGGTAC
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.879_880insAGGTAC
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1020_1021insAGGTAC
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.957_958insAGGTAC
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1083_1084insAGGTAC
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1212_1213insAGGTAC
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu404_Ser405insArgTyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

8-11696077-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696077
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696077
    reference: chr 8
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.958T>C
  hgvsp: ENSP00000431649.1:p.Ser320Pro
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.958T>C
  hgvsp: ENSP00000436069.1:p.Ser320Pro
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.916T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1491T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1021T>C
  hgvsp: ENSP00000432331.1:p.Ser341Pro
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1213T>C
  hgvsp: ENSP00000220584.4:p.Ser405Pro
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1084T>C
  hgvsp: ENSP00000390367.2:p.Ser362Pro
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1192T>C
  hgvsp: ENSP00000434714.1:p.Ser398Pro
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.880T>C
  hgvsp: ENSP00000444248.1:p.Ser294Pro
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1021T>C
  hgvsp: ENSP00000431749.1:p.Ser341Pro
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1272T>C
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser405Pro
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/8-11696078-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696078
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696078
    reference: chr 8
allele count: 1
allele frequency: 8.258456659619451e-6
allele num: 121088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.881C>A
  hgvsp: ENSP00000444248.1:p.Ser294Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1193C>A
  hgvsp: ENSP00000434714.1:p.Ser398Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.917C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1492C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.959C>A
  hgvsp: ENSP00000431649.1:p.Ser320Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.959C>A
  hgvsp: ENSP00000436069.1:p.Ser320Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1085C>A
  hgvsp: ENSP00000390367.2:p.Ser362Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1022C>A
  hgvsp: ENSP00000432331.1:p.Ser341Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1273C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1214C>A
  hgvsp: ENSP00000220584.4:p.Ser405Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1022C>A
  hgvsp: ENSP00000431749.1:p.Ser341Tyr
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser405Tyr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

8-11696078-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696078
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696078
    reference: chr 8
allele count: 1
allele frequency: 8.258456659619451e-6
allele num: 121088
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1022C>G
  hgvsp: ENSP00000431749.1:p.Ser341Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1273C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.959C>G
  hgvsp: ENSP00000436069.1:p.Ser320Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.959C>G
  hgvsp: ENSP00000431649.1:p.Ser320Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1022C>G
  hgvsp: ENSP00000432331.1:p.Ser341Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1085C>G
  hgvsp: ENSP00000390367.2:p.Ser362Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1193C>G
  hgvsp: ENSP00000434714.1:p.Ser398Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.881C>G
  hgvsp: ENSP00000444248.1:p.Ser294Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1214C>G
  hgvsp: ENSP00000220584.4:p.Ser405Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.917C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1492C>G
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser405Cys
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-11696079-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696079
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696079
    reference: chr 8
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1194C>G
  hgvsp: ENST00000525900.1:c.1194C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1023C>G
  hgvsp: ENST00000528812.1:c.1023C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.960C>G
  hgvsp: ENST00000528643.1:c.960C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1274C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1023C>G
  hgvsp: ENST00000530664.1:c.1023C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1215C>G
  hgvsp: ENST00000220584.4:c.1215C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.918C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.882C>G
  hgvsp: ENST00000538689.1:c.882C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1086C>G
  hgvsp: ENST00000443614.2:c.1086C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1493C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.960C>G
  hgvsp: ENST00000525777.1:c.960C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser405Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum

8-11696081-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696081
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696081
    reference: chr 8
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1495A>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.962A>T
  hgvsp: ENSP00000431649.1:p.Gln321Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1025A>T
  hgvsp: ENSP00000432331.1:p.Gln342Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1196A>T
  hgvsp: ENSP00000434714.1:p.Gln399Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1276A>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1088A>T
  hgvsp: ENSP00000390367.2:p.Gln363Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.962A>T
  hgvsp: ENSP00000436069.1:p.Gln321Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.884A>T
  hgvsp: ENSP00000444248.1:p.Gln295Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1025A>T
  hgvsp: ENSP00000431749.1:p.Gln342Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1217A>T
  hgvsp: ENSP00000220584.4:p.Gln406Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.920A>T
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln406Leu
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

8-11696082-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696082
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696082
    reference: chr 8
allele count: 2
allele frequency: 1.650491846570278e-5
allele num: 121176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1026G>A
  hgvsp: ENST00000528812.1:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1197G>A
  hgvsp: ENST00000525900.1:c.1197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1277G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.921G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1496G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1026G>A
  hgvsp: ENST00000530664.1:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.963G>A
  hgvsp: ENST00000525777.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1089G>A
  hgvsp: ENST00000443614.2:c.1089G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.885G>A
  hgvsp: ENST00000538689.1:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.963G>A
  hgvsp: ENST00000528643.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1218G>A
  hgvsp: ENST00000220584.4:c.1218G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12446
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln406Gln
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-11696082-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696082
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696082
    reference: chr 8
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1496G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1089G>C
  hgvsp: ENSP00000390367.2:p.Gln363His
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.963G>C
  hgvsp: ENSP00000431649.1:p.Gln321His
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.885G>C
  hgvsp: ENSP00000444248.1:p.Gln295His
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1026G>C
  hgvsp: ENSP00000431749.1:p.Gln342His
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1277G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1197G>C
  hgvsp: ENSP00000434714.1:p.Gln399His
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.921G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1218G>C
  hgvsp: ENSP00000220584.4:p.Gln406His
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.963G>C
  hgvsp: ENSP00000436069.1:p.Gln321His
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1026G>C
  hgvsp: ENSP00000432331.1:p.Gln342His
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln406His
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-11696082-G-GGT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696082
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696084
    reference: chr 8
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: GGT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1090_1091dupGT
  hgvsp: ENSP00000390367.2:p.Thr365Ter
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1027_1028dupGT
  hgvsp: ENSP00000431749.1:p.Thr344Ter
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1497_1498dupGT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.964_965dupGT
  hgvsp: ENSP00000436069.1:p.Thr323Ter
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.886_887dupGT
  hgvsp: ENSP00000444248.1:p.Thr297Ter
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.964_965dupGT
  hgvsp: ENSP00000431649.1:p.Thr323Ter
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1278_*1279dupGT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1198_1199dupGT
  hgvsp: ENSP00000434714.1:p.Thr401Ter
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1027_1028dupGT
  hgvsp: ENSP00000432331.1:p.Thr344Ter
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1219_1220dupGT
  hgvsp: ENSP00000220584.4:p.Thr408Ter
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.922_923dupGT
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr408Ter
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

8-11696083-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696083
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696083
    reference: chr 8
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.964G>C
  hgvsp: ENSP00000431649.1:p.Val322Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1219G>C
  hgvsp: ENSP00000220584.4:p.Val407Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1027G>C
  hgvsp: ENSP00000431749.1:p.Val343Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.886G>C
  hgvsp: ENSP00000444248.1:p.Val296Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1278G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1198G>C
  hgvsp: ENSP00000434714.1:p.Val400Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1090G>C
  hgvsp: ENSP00000390367.2:p.Val364Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1497G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.964G>C
  hgvsp: ENSP00000436069.1:p.Val322Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1027G>C
  hgvsp: ENSP00000432331.1:p.Val343Leu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.922G>C
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val407Leu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

8-11696087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696087
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696087
    reference: chr 8
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1282C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.968C>T
  hgvsp: ENSP00000431649.1:p.Thr323Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.968C>T
  hgvsp: ENSP00000436069.1:p.Thr323Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1223C>T
  hgvsp: ENSP00000220584.4:p.Thr408Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1202C>T
  hgvsp: ENSP00000434714.1:p.Thr401Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1094C>T
  hgvsp: ENSP00000390367.2:p.Thr365Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.890C>T
  hgvsp: ENSP00000444248.1:p.Thr297Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1031C>T
  hgvsp: ENSP00000432331.1:p.Thr344Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1501C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.926C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1031C>T
  hgvsp: ENSP00000431749.1:p.Thr344Ile
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr408Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-11696094-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696094
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696094
    reference: chr 8
allele count: 2
allele frequency: 1.649103712132456e-5
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.933C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1038C>G
  hgvsp: ENSP00000431749.1:p.Asp346Glu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.975C>G
  hgvsp: ENSP00000431649.1:p.Asp325Glu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1209C>G
  hgvsp: ENSP00000434714.1:p.Asp403Glu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1230C>G
  hgvsp: ENSP00000220584.4:p.Asp410Glu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1508C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1101C>G
  hgvsp: ENSP00000390367.2:p.Asp367Glu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.897C>G
  hgvsp: ENSP00000444248.1:p.Asp299Glu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.975C>G
  hgvsp: ENSP00000436069.1:p.Asp325Glu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1038C>G
  hgvsp: ENSP00000432331.1:p.Asp346Glu
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1289C>G
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp410Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

8-11696094-CTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696094
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696092
    reference: chr 8
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1040_1041delAT
  hgvsp: ENSP00000431749.1:p.Tyr347CysfsTer41
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1291_*1292delAT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1510_1511delAT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1211_1212delAT
  hgvsp: ENSP00000434714.1:p.Tyr404CysfsTer41
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1232_1233delAT
  hgvsp: ENSP00000220584.4:p.Tyr411CysfsTer41
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.977_978delAT
  hgvsp: ENSP00000436069.1:p.Tyr326CysfsTer?
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.899_900delAT
  hgvsp: ENSP00000444248.1:p.Tyr300CysfsTer41
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1040_1041delAT
  hgvsp: ENSP00000432331.1:p.Tyr347CysfsTer41
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.935_936delAT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.977_978delAT
  hgvsp: ENSP00000431649.1:p.Tyr326CysfsTer41
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1103_1104delAT
  hgvsp: ENSP00000390367.2:p.Tyr368CysfsTer41
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr411CysfsTer41
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: CTA
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

8-11696096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696096
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696096
    reference: chr 8
allele count: 4
allele frequency: 3.297935492381769e-5
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.935A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.899A>G
  hgvsp: ENSP00000444248.1:p.Tyr300Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1211A>G
  hgvsp: ENSP00000434714.1:p.Tyr404Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.977A>G
  hgvsp: ENSP00000436069.1:p.Tyr326Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.977A>G
  hgvsp: ENSP00000431649.1:p.Tyr326Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1291A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1040A>G
  hgvsp: ENSP00000432331.1:p.Tyr347Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1510A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1040A>G
  hgvsp: ENSP00000431749.1:p.Tyr347Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1232A>G
  hgvsp: ENSP00000220584.4:p.Tyr411Cys
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1103A>G
  hgvsp: ENSP00000390367.2:p.Tyr368Cys
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr411Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

8-11696098-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696098
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696098
    reference: chr 8
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.979G>A
  hgvsp: ENSP00000436069.1:p.Val327Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1234G>A
  hgvsp: ENSP00000220584.4:p.Val412Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.901G>A
  hgvsp: ENSP00000444248.1:p.Val301Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1213G>A
  hgvsp: ENSP00000434714.1:p.Val405Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1042G>A
  hgvsp: ENSP00000432331.1:p.Val348Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1512G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1105G>A
  hgvsp: ENSP00000390367.2:p.Val369Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.937G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.979G>A
  hgvsp: ENSP00000431649.1:p.Val327Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1042G>A
  hgvsp: ENSP00000431749.1:p.Val348Ile
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1293G>A
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val412Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

8-11696113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696113
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696113
    reference: chr 8
allele count: 5
allele frequency: 4.12173970389422e-5
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1249C>T
  hgvsp: ENSP00000220584.4:p.His417Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1228C>T
  hgvsp: ENSP00000434714.1:p.His410Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.952C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.994C>T
  hgvsp: ENSP00000431649.1:p.His332Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1057C>T
  hgvsp: ENSP00000432331.1:p.His353Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1308C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.994C>T
  hgvsp: ENSP00000436069.1:p.His332Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1120C>T
  hgvsp: ENSP00000390367.2:p.His374Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1057C>T
  hgvsp: ENSP00000431749.1:p.His353Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.916C>T
  hgvsp: ENSP00000444248.1:p.His306Tyr
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1527C>T
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His417Tyr
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/8-11696113-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696113
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696113
    reference: chr 8
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.994C>A
  hgvsp: ENSP00000431649.1:p.His332Asn
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1228C>A
  hgvsp: ENSP00000434714.1:p.His410Asn
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1120C>A
  hgvsp: ENSP00000390367.2:p.His374Asn
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1057C>A
  hgvsp: ENSP00000432331.1:p.His353Asn
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.952C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1057C>A
  hgvsp: ENSP00000431749.1:p.His353Asn
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1249C>A
  hgvsp: ENSP00000220584.4:p.His417Asn
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1527C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1308C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.994C>A
  hgvsp: ENSP00000436069.1:p.His332Asn
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.916C>A
  hgvsp: ENSP00000444248.1:p.His306Asn
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His417Asn
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

8-11696115-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696115
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696115
    reference: chr 8
allele count: 252
allele frequency: 2.077493816982687e-3
allele num: 121300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1059C>G
  hgvsp: ENSP00000431749.1:p.His353Gln
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.918C>G
  hgvsp: ENSP00000444248.1:p.His306Gln
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.996C>G
  hgvsp: ENSP00000436069.1:p.His332Gln
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.954C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1059C>G
  hgvsp: ENSP00000432331.1:p.His353Gln
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1251C>G
  hgvsp: ENSP00000220584.4:p.His417Gln
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1529C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.996C>G
  hgvsp: ENSP00000431649.1:p.His332Gln
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1310C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1122C>G
  hgvsp: ENSP00000390367.2:p.His374Gln
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1230C>G
  hgvsp: ENSP00000434714.1:p.His410Gln
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 12491
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22933
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.His417Gln
num of homozygotes: 4
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

8-11696118-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696118
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696118
    reference: chr 8
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.1233A>T
  hgvsp: ENSP00000434714.1:p.Ter411CysextTer6
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.1062A>T
  hgvsp: ENSP00000432331.1:p.Ter354CysextTer6
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.999A>T
  hgvsp: ENSP00000436069.1:p.Ter333CysextTer?
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.921A>T
  hgvsp: ENSP00000444248.1:p.Ter307CysextTer6
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.957A>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.1062A>T
  hgvsp: ENSP00000431749.1:p.Ter354CysextTer6
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.1125A>T
  hgvsp: ENSP00000390367.2:p.Ter375CysextTer6
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.999A>T
  hgvsp: ENSP00000431649.1:p.Ter333CysextTer6
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1532A>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1313A>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.1254A>T
  hgvsp: ENSP00000220584.4:p.Ter418CysextTer6
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter418CysextTer6
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-11696120-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696120
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696120
    reference: chr 8
allele count: 3
allele frequency: 2.473492406378312e-5
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*2C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*2C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*2C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1315C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*2C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.959C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*2C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*2C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*2C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1534C>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.*2C>A
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12569
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

8-11696120-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696120
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696120
    reference: chr 8
allele count: 6
allele frequency: 4.946984812756625e-5
allele num: 121286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*2C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*2C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*2C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*2C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*2C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.959C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*2C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*2C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1315C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.*2C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1534C>G
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12569
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

8-11696120-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696120
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696120
    reference: chr 8
allele count: 2
allele frequency: 1.648994937585542e-5
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1315C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.959C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*2C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*2C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1534C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12569
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

8-11696122-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696122
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696122
    reference: chr 8
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*4C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000436069
  ensembl transcript: ENST00000525777
  gene symbol: FDFT1
  hgvsc: ENST00000525777.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*4C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1317C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*4C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.961C>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1536C>T
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12557
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

8-11696129-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696129
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696129
    reference: chr 8
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*11G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*11G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*11G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1543G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*11G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*11G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*11G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*11G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1324G>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.968G>C
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

8-11696130-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696130
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696130
    reference: chr 8
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*12T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*12T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*12T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1544T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*12T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*12T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.969T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*12T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*12T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1325T>C
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12539
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

8-11696131-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696131
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696131
    reference: chr 8
allele count: 4
allele frequency: 3.302455375571737e-5
allele num: 121122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*13C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*13C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*13C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*13C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1326C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*13C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*13C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*13C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.970C>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1545C>G
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8431
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40322
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

8-11696133-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696133
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696133
    reference: chr 8
allele count: 2
allele frequency: 1.652046059044126e-5
allele num: 121062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*15A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*15A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.972A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*15A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1328A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*15A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*15A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*15A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*15A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1547A>G
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16801
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

8-11696139-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696139
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696139
    reference: chr 8
allele count: 1
allele frequency: 8.274446853227862e-6
allele num: 120854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.978G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*21G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*21G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1334G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1553G>A
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

8-11696142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696142
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696142
    reference: chr 8
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*24G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.981G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*24G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1337G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1556G>A
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

8-11696142-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696142
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696142
    reference: chr 8
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*24G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*24G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.981G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*24G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*24G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1337G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*24G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*24G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*24G>T
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1556G>T
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3645
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

8-11696149-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696149
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696149
    reference: chr 8
allele count: 2
allele frequency: 1.66281447978849e-5
allele num: 120278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*31A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.988A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*31A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1344A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*31A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*31A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*31A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*31A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*31A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1563A>G
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7287
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3638
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ

8-11696155-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696155
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696155
    reference: chr 8
allele count: 2
allele frequency: 1.667000066680003e-5
allele num: 119976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1569T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*37T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*37T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*37T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*37T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*37T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*37T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1350T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.994T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*37T>C
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2028
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

8-11696162-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696162
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696162
    reference: chr 8
allele count: 1
allele frequency: 8.391232839928842e-6
allele num: 119172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*44A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*44A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*44A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*44A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1357A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*44A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1576A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*44A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*44A>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.1001A>G
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11725
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3636
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

8-11696163-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696163
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696164
    reference: chr 8
allele count: 2
allele frequency: 1.691103106556407e-5
allele num: 118266
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*52dupT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*52dupT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*52dupT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*52dupT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.1009dupT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*52dupT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1365dupT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1584dupT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*52dupT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*52dupT
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16995
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12089
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

8-11696165-TTTTTTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696165
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696159
    reference: chr 8
allele count: 1
allele frequency: 8.43810648890389e-6
allele num: 118510
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*51_*56delTTCTTT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*51_*56delTTCTTT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1583_1588delTTCTTT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.1008_1013delTTCTTT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*51_*56delTTCTTT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*51_*56delTTCTTT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*51_*56delTTCTTT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*51_*56delTTCTTT
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*51_*56delTTCTTT
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2107
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4058
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: TTTTTTC
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-11696168-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696168
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696168
    reference: chr 8
allele count: 3
allele frequency: 2.544874622510264e-5
allele num: 117884
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*50T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.1007T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*50T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*50T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*50T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1582T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*50T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*50T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*50T>C
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1363T>C
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17871
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12832
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6361
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

8-11696169-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11696169
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11696169
    reference: chr 8
allele count: 1
allele frequency: 8.505281779985371e-6
allele num: 117574
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431749
  ensembl transcript: ENST00000528812
  gene symbol: FDFT1
  hgvsc: ENST00000528812.1:c.*51T>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432331
  ensembl transcript: ENST00000530664
  gene symbol: FDFT1
  hgvsc: ENST00000530664.1:c.*51T>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000444248
  ensembl transcript: ENST00000538689
  gene symbol: FDFT1
  hgvsc: ENST00000538689.1:c.*51T>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000220584
  ensembl transcript: ENST00000220584
  gene symbol: FDFT1
  hgvsc: ENST00000220584.4:c.*51T>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000432551
  ensembl transcript: ENST00000525607
  gene symbol: FDFT1
  hgvsc: ENST00000525607.1:c.*1364T>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000431649
  ensembl transcript: ENST00000528643
  gene symbol: FDFT1
  hgvsc: ENST00000528643.1:c.*51T>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000434714
  ensembl transcript: ENST00000525900
  gene symbol: FDFT1
  hgvsc: ENST00000525900.1:c.*51T>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000446331
  gene symbol: FDFT1
  hgvsc: ENST00000446331.2:n.1008T>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000079459
  ensembl protein: ENSP00000390367
  ensembl transcript: ENST00000443614
  gene symbol: FDFT1
  hgvsc: ENST00000443614.2:c.*51T>G
  variant of: http://identifiers.org/hgnc/3629
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079459
  ensembl transcript: ENST00000525954
  gene symbol: FDFT1
  hgvsc: ENST00000525954.1:n.1583T>G
  variant of: http://identifiers.org/hgnc/3629
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11557
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4912
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3488
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

8-11702584-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702584
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702584
    reference: chr 8
allele count: 1
allele frequency: 8.9394264463992e-6
allele num: 111864
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*50A>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*618A>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*43+7A>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*43+7A>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*50A>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*43+7A>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*618A>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1175A>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*50A>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*50A>G
  variant of: http://identifiers.org/hgnc/2527
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14868
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12775
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*43+7A>G
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-11702590-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702590
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702590
    reference: chr 8
allele count: 1
allele frequency: 8.893315783856854e-6
allele num: 112444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*43+1G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*44G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*44G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*44G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*43+1G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*612G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1169G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*43+1G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*44G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*44G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*44G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*612G>C
  variant of: http://identifiers.org/hgnc/2527
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8794
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*43+1G>C
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

8-11702593-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702593
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702593
    reference: chr 8
allele count: 3
allele frequency: 2.66018763190097e-5
allele num: 112774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*41G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*41G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*41G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1166G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*41G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*609G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*41G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*41G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*41G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*41G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*41G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*609G>A
  variant of: http://identifiers.org/hgnc/2527
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*41G>A
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

8-11702594-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702594
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702594
    reference: chr 8
allele count: 22893
allele frequency: 2.00096145441832e-1
allele num: 114410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*40C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*40C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*40C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*40C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*40C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*608C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*608C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*40C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*40C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1165C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*40C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*40C>G
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7186
  bin: 1.25e1
  variant carriers: 1606
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 9.75e1
  variant carriers: 217
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 1.75e1
  variant carriers: 3713
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.25e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 3.25e1
  variant carriers: 2428
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 403
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 932
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 286
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 7.5e0
  variant carriers: 260
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 3.75e1
  variant carriers: 1548
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.75e1
  variant carriers: 631
genotype depth: GenotypeDepth
  all individuals: 21263
  bin: 2.25e1
  variant carriers: 4321
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 196
genotype quality: GenotypeQuality
num of homozygotes: 2582
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

8-11702596-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702596
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702596
    reference: chr 8
allele count: 1
allele frequency: 8.637965586345104e-6
allele num: 115768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*38A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*38A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*38A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*38A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*606A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*38A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*38A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*606A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1163A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*38A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*38A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*38A>T
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14168
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-11702598-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702598
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702598
    reference: chr 8
allele count: 29
allele frequency: 2.500991772599479e-4
allele num: 115954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*604A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*36A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*36A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*36A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*604A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*36A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*36A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*36A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*36A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*36A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*36A>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1161A>T
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24956
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14401
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 2
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/8-11702599-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702599
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702599
    reference: chr 8
allele count: 1
allele frequency: 8.623217149854268e-6
allele num: 115966
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*35G>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*603G>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*35G>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1160G>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*603G>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*35G>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*35G>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*35G>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*35G>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*35G>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*35G>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*35G>T
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-11702599-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702599
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702599
    reference: chr 8
allele count: 3
allele frequency: 2.58696514495628e-5
allele num: 115966
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*603G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*35G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*35G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1160G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*35G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*35G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*35G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*35G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*35G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*603G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*35G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*35G>A
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25422
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

8-11702600-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702600
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702600
    reference: chr 8
allele count: 3
allele frequency: 2.58215558348109e-5
allele num: 116182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*602C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*34C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*34C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*34C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*34C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1159C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*34C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*602C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26218
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

8-11702601-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702601
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702601
    reference: chr 8
allele count: 3
allele frequency: 2.575018883471812e-5
allele num: 116504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*601G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*33G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*601G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*33G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*33G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*33G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*33G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1158G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*33G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*33G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*33G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*33G>A
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26816
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15127
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

8-11702602-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702602
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702602
    reference: chr 8
allele count: 2
allele frequency: 1.713619850572349e-5
allele num: 116712
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*32G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*600G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*32G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*32G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*32G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*32G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*32G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*32G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*600G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*32G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1157G>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*32G>A
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4536
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

8-11702605-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702605
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702605
    reference: chr 8
allele count: 9
allele frequency: 7.679836163495179e-5
allele num: 117190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*29G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*29G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*29G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*29G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*29G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*29G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1154G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*29G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*597G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*29G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*597G>C
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*29G>C
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28297
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

8-11702607-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702607
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702607
    reference: chr 8
allele count: 1
allele frequency: 8.509479560230096e-6
allele num: 117516
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*27C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*595C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*27C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*27C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*27C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*27C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*27C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*27C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1152C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*595C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*27C>T
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*27C>T
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

8-11702608-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702608
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702608
    reference: chr 8
allele count: 1
allele frequency: 8.500799075113061e-6
allele num: 117636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*26C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*26C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*26C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*594C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*26C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*26C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1151C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*26C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*26C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*26C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*26C>G
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*594C>G
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

8-11702608-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702608
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702608
    reference: chr 8
allele count: 8
allele frequency: 6.800639260090449e-5
allele num: 117636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*26C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*594C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*26C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*26C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*26C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*26C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*26C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*26C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1151C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*594C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*26C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*26C>A
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28845
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-11702613-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11702613
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 11702613
    reference: chr 8
allele count: 1
allele frequency: 8.470412847922207e-6
allele num: 118058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000433215
  ensembl transcript: ENST00000531089
  gene symbol: CTSB
  hgvsc: ENST00000531089.1:c.*21C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000409917
  ensembl transcript: ENST00000453527
  gene symbol: CTSB
  hgvsc: ENST00000453527.2:c.*21C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000432244
  ensembl transcript: ENST00000533455
  gene symbol: CTSB
  hgvsc: ENST00000533455.1:c.*21C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000345672
  ensembl transcript: ENST00000353047
  gene symbol: CTSB
  hgvsc: ENST00000353047.6:c.*21C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000435105
  ensembl transcript: ENST00000530640
  gene symbol: CTSB
  hgvsc: ENST00000530640.2:c.*21C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000411254
  ensembl transcript: ENST00000415599
  gene symbol: CTSB
  hgvsc: ENST00000415599.2:c.*589C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000164733
  ensembl transcript: ENST00000420692
  gene symbol: CTSB
  hgvsc: ENST00000420692.2:n.1146C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000434217
  ensembl transcript: ENST00000534510
  gene symbol: CTSB
  hgvsc: ENST00000534510.1:c.*21C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000473301
  ensembl transcript: ENST00000526481
  gene symbol: CTSB
  hgvsc: ENST00000526481.2:c.*21C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000436456
  ensembl transcript: ENST00000531551
  gene symbol: CTSB
  hgvsc: ENST00000531551.1:c.*589C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000342070
  ensembl transcript: ENST00000345125
  gene symbol: CTSB
  hgvsc: ENST00000345125.3:c.*21C>A
  variant of: http://identifiers.org/hgnc/2527
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000164733
  ensembl protein: ENSP00000415889
  ensembl transcript: ENST00000434271
  gene symbol: CTSB
  hgvsc: ENST00000434271.1:c.*21C>A
  variant of: http://identifiers.org/hgnc/2527
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16675
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 79
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2198
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7902
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38522
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1941
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3879
bin: 9.75e1
variant carriers: 1

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: 11566
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.499415052645263e-5
allele num: 15386
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: 0
allele frequency: 0.0e0
allele num: 66338
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.99e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.518e-1

QD
type: SiteQuality
SIO_000300: 2.145e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

FS
type: SiteQuality
SIO_000300: 1.385e0

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.25e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

DP
type: SiteQuality
SIO_000300: 1.741664e6

GenotypeDepth
all individuals: 3177
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7922
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3878
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 38683
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 360
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66344
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.476683937823834e-5
allele num: 15440
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: 10400
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

DP
type: SiteQuality
SIO_000300: 1.74258e6

QD
type: SiteQuality
SIO_000300: 1.343e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.7e0

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeDepth
all individuals: 114
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7948
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3880
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 748
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38740
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66358
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
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: 15506
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.44e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.14e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

MQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

FS
type: SiteQuality
SIO_000300: 7.248e0

QD
type: SiteQuality
SIO_000300: 1.41e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

DP
type: SiteQuality
SIO_000300: 1.743992e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.38e-1

GenotypeDepth
all individuals: 282
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3880
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7948
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.013954609843576e-5
allele num: 66358
num of homozygotes: 0

Latino
type: Population
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num of homozygotes: 0

East Asian
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allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
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MQRankSum
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SIO_000300: 7.55e-1

FS
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DP
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ReadPosRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -4.38e-1

VQSLOD
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SIO_000300: 5.14e-1

MQ
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SIO_000300: 5.978e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 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 frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66350
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Latino
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South Asian
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Other
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DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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FS
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MQ
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SIO_000300: 5.974e1

BaseQRankSum
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ClippingRankSum
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SIO_000300: -1.09e-1

GenotypeDepth
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variant carriers: 0

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

African
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Latino
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European (Finnish)
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele num: 66350
num of homozygotes: 0

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

GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele num: 10400
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Other
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South Asian
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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VQSLOD
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FS
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MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 8.179999999999999e-1

ClippingRankSum
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

South Asian
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allele frequency: 6.422607578676943e-5
allele num: 15570
num of homozygotes: 0

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

Other
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East Asian
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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FS
type: SiteQuality
SIO_000300: 0.0e0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66434
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

African
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Other
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South Asian
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European (Finnish)
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DP
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ClippingRankSum
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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allele num: 15854
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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ClippingRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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MQ
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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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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 frequency: 1.503759398496241e-5
allele num: 66500
num of homozygotes: 0

African
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Latino
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Other
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European (Finnish)
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East Asian
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South Asian
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VQSLOD
type: SiteQuality
SIO_000300: 9.379999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.303e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

FS
type: SiteQuality
SIO_000300: 2.676e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.143e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 1.761097e6

GenotypeDepth
all individuals: 1321
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
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GenotypeQuality
all individuals: 8233
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1353
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2323
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39766
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4034
bin: 9.75e1
variant carriers: 228

GenotypeQuality
all individuals: 544
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.251562890722681e-5
allele num: 15996
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.513825438807405e-5
allele num: 66544
num of homozygotes: 0

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

Latino
type: Population
allele count: 8
allele frequency: 6.912044237083118e-4
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
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: 216
allele frequency: 2.075725542955987e-2
allele num: 10406
num of homozygotes: 3

VQSLOD
type: SiteQuality
SIO_000300: 6.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.581e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.77e-2

MQ
type: SiteQuality
SIO_000300: 5.981e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

DP
type: SiteQuality
SIO_000300: 1.778493e6

QD
type: SiteQuality
SIO_000300: 1.349e1

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
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variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 163
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variant carriers: 0

GenotypeQuality
all individuals: 150
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variant carriers: 0

GenotypeQuality
all individuals: 39906
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variant carriers: 0

GenotypeQuality
all individuals: 1392
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variant carriers: 0

GenotypeQuality
all individuals: 552
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GenotypeQuality
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GenotypeQuality
all individuals: 436
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 8342
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3842
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.25e1
variant carriers: 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: 10406
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16120
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004175804368072e-5
allele num: 66574
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.769393e6

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.95e-1

FS
type: SiteQuality
SIO_000300: 8.333e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

QD
type: SiteQuality
SIO_000300: 1.133e1

GenotypeDepth
all individuals: 66
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40092
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 145
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 8391
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 390
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variant carriers: 0

GenotypeQuality
all individuals: 128
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GenotypeQuality
all individuals: 1409
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 556
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GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 3844
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 117
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variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2391
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.034e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.53e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.132e1

DP
type: SiteQuality
SIO_000300: 1.77099e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

GenotypeDepth
all individuals: 78
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2406
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 359
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variant carriers: 0

GenotypeQuality
all individuals: 3844
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 128
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 8416
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 40171
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 2127
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 777
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variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16196
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

QD
type: SiteQuality
SIO_000300: 1.158e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 3.224e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.772331e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.749e0

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.79e-1

GenotypeQuality
all individuals: 560
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 1427
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 2424
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40256
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variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 0
bin: 1.25e1
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GenotypeQuality
all individuals: 780
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GenotypeQuality
all individuals: 2142
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8436
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3846
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 1
allele frequency: 6.159152500615915e-5
allele num: 16236
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: -4.69e0

QD
type: SiteQuality
SIO_000300: 9.15e0

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 1.915e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-1

MQ
type: SiteQuality
SIO_000300: 5.165e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.149999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.773838e6

GenotypeDepth
all individuals: 66
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 39
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 781
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variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
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: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.39e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e-1

DP
type: SiteQuality
SIO_000300: 1.775463e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 7.617e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 548
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 241
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 782
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 34
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1443
bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16292
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

DP
type: SiteQuality
SIO_000300: 1.776146e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
SIO_000300: 1.436e1

MQRankSum
type: SiteQuality
SIO_000300: -1.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.45e-1

GenotypeDepth
all individuals: 12395
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
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variant carriers: 0

GenotypeQuality
all individuals: 34
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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Latino
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FS
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QD
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MQRankSum
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BaseQRankSum
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DP
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MQ
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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South Asian
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MQ
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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InbreedingCoeff
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QD
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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InbreedingCoeff
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MQ
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QD
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DP
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FS
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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FS
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InbreedingCoeff
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VQSLOD
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DP
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QD
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MQ
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ReadPosRankSum
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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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European (Non-Finnish)
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South Asian
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African
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FS
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QD
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DP
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MQ
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InbreedingCoeff
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South Asian
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European (Non-Finnish)
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FS
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MQ
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InbreedingCoeff
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African
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East Asian
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele count: 1
allele frequency: 6.095330976472023e-5
allele num: 16406
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

MQ
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SIO_000300: 5.974e1

InbreedingCoeff
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QD
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MQRankSum
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VQSLOD
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DP
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SIO_000300: 1.780471e6

FS
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SIO_000300: 2.02e0

BaseQRankSum
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SIO_000300: -5.045e0

ClippingRankSum
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SIO_000300: 8.139999999999999e-1

ReadPosRankSum
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SIO_000300: -1.014e0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
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 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 (Non-Finnish)
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allele count: 2
allele frequency: 2.999400119976005e-5
allele num: 66680
num of homozygotes: 0

South Asian
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Other
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ClippingRankSum
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SIO_000300: 9.31e-1

ReadPosRankSum
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BaseQRankSum
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MQRankSum
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MQ
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FS
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VQSLOD
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InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

DP
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SIO_000300: 1.781866e6

QD
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SIO_000300: 1.639e1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 582
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

Other
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num of homozygotes: 0

East Asian
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MQRankSum
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SIO_000300: 1.6e0

BaseQRankSum
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FS
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QD
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ReadPosRankSum
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SIO_000300: 4.81e-1

MQ
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InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

VQSLOD
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DP
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SIO_000300: 1.781866e6

ClippingRankSum
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SIO_000300: 9.31e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
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: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

South Asian
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VQSLOD
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SIO_000300: 1.49e0

MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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MQ
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SIO_000300: 5.937e1

ClippingRankSum
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SIO_000300: -2.1e-1

QD
type: SiteQuality
SIO_000300: 6.46e0

DP
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SIO_000300: 1.782252e6

InbreedingCoeff
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SIO_000300: 5.0e-4

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
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

African
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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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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

Other
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ReadPosRankSum
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SIO_000300: 1.21e0

MQ
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InbreedingCoeff
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DP
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VQSLOD
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FS
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: -8.9e-1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
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allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 5.998260504453708e-5
allele num: 66686
num of homozygotes: 0

South Asian
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Other
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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FS
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QD
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MQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 906
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Latino
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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: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

East Asian
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South Asian
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BaseQRankSum
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QD
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ClippingRankSum
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DP
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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VQSLOD
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ReadPosRankSum
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SIO_000300: 6.8e-1

GenotypeDepth
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variant carriers: 16

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1474
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GenotypeQuality
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variant carriers: 246

GenotypeQuality
all individuals: 2495
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GenotypeQuality
all individuals: 587
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variant carriers: 0

East Asian
type: Population
allele count: 239
allele frequency: 2.764284061993986e-2
allele num: 8646
num of homozygotes: 4

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 12
allele frequency: 7.274490785645005e-4
allele num: 16496
num of homozygotes: 0

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

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

ReadPosRankSum
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SIO_000300: 5.01e-1

FS
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SIO_000300: 1.627e0

InbreedingCoeff
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SIO_000300: 2.58e-2

QD
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BaseQRankSum
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SIO_000300: -1.703e0

DP
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SIO_000300: 1.783572e6

MQRankSum
type: SiteQuality
SIO_000300: 2.76e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-2

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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ClippingRankSum
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SIO_000300: 1.1e0

ReadPosRankSum
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InbreedingCoeff
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FS
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SIO_000300: 1.126e0

QD
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SIO_000300: 1.516e1

MQ
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SIO_000300: 5.875e1

MQRankSum
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SIO_000300: 9.399999999999999e-1

VQSLOD
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SIO_000300: -6.607e-1

DP
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SIO_000300: 1.774728e6

BaseQRankSum
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SIO_000300: 4.17e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.499370088187654e-5
allele num: 66676
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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MQ
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SIO_000300: 5.96e1

BaseQRankSum
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SIO_000300: 7.49e-1

InbreedingCoeff
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SIO_000300: 4.0e-4

MQRankSum
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SIO_000300: 5.669999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.428e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

DP
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SIO_000300: 1.774708e6

QD
type: SiteQuality
SIO_000300: 1.326e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.75e1
variant carriers: 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: 16498
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.498950146979423e-5
allele num: 66676
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.428e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.96e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.774708e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
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: 10390
num of homozygotes: 0

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

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

South Asian
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allele frequency: 6.06134076857801e-5
allele num: 16498
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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SIO_000300: 1.774708e6

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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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: 6606
num of homozygotes: 0

East Asian
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allele count: 1
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allele num: 8652
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11536
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
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.663e0

ClippingRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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QD
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BaseQRankSum
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MQRankSum
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SIO_000300: 6.41e-1

DP
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SIO_000300: 1.773737e6

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

European (Non-Finnish)
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allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

European (Finnish)
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Latino
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African
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South Asian
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East Asian
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Other
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DP
type: SiteQuality
SIO_000300: 1.769739e6

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.5008254539997e-5
allele num: 66630
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Other
type: Population
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African
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South Asian
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Latino
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allele count: 3
allele frequency: 2.605976372480889e-4
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

BaseQRankSum
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SIO_000300: 3.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.605e1

FS
type: SiteQuality
SIO_000300: 1.474e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

DP
type: SiteQuality
SIO_000300: 1.769167e6

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: 2

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.316423442205235e-4
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.12e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -9.49e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

DP
type: SiteQuality
SIO_000300: 1.766531e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 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: 10320
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.081245439065921e-5
allele num: 16444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.236e0

QD
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SIO_000300: 1.532e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.078e0

DP
type: SiteQuality
SIO_000300: 1.755982e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8093
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505888022166672e-5
allele num: 66406
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.984e1

QD
type: SiteQuality
SIO_000300: 1.326e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.141e0

VQSLOD
type: SiteQuality
SIO_000300: 8.34e-1

DP
type: SiteQuality
SIO_000300: 1.74135e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
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: 10316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505888022166672e-5
allele num: 66406
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.74135e6

MQRankSum
type: SiteQuality
SIO_000300: 9.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.141e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.326e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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
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num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.21921482565228e-4
allele num: 16404
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8500
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.24e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
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InbreedingCoeff
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QD
type: SiteQuality
SIO_000300: 1.334e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

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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variant carriers: 2

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.027367401307823e-5
allele num: 66064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523182842868458e-5
allele num: 65652
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
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Other
type: Population
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allele frequency: 0.0e0
allele num: 894
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6548
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

VQSLOD
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MQ
type: SiteQuality
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DP
type: SiteQuality
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FS
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2290
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GenotypeQuality
all individuals: 2354
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.150061500615006e-5
allele num: 16260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534872298624754e-5
allele num: 65152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11184
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.61e-1

DP
type: SiteQuality
SIO_000300: 1.517082e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.823e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 6.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

GenotypeQuality
all individuals: 6259
bin: 3.75e1
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: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.139489194499017e-5
allele num: 16288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11208
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65296
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

QD
type: SiteQuality
SIO_000300: 5.17e0

DP
type: SiteQuality
SIO_000300: 1.515427e6

MQRankSum
type: SiteQuality
SIO_000300: -4.275e0

FS
type: SiteQuality
SIO_000300: 1.585e0

MQ
type: SiteQuality
SIO_000300: 5.243e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.11e-1

GenotypeQuality
all individuals: 4123
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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: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11140
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.991635132443736e-4
allele num: 10042
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540167570231641e-5
allele num: 64928
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.889e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.506534e6

VQSLOD
type: SiteQuality
SIO_000300: -2.01e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

QD
type: SiteQuality
SIO_000300: 1.817e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4220
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1355
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11102
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.000200040008002e-4
allele num: 9998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8068
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64756
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.254e-1

QD
type: SiteQuality
SIO_000300: 1.791e1

DP
type: SiteQuality
SIO_000300: 1.505636e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 216
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variant carriers: 0

GenotypeDepth
all individuals: 80
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 13168
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GenotypeQuality
all individuals: 3567
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.643871646501841e-5
allele num: 60832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8212
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15462
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.35e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: -2.072e0

DP
type: SiteQuality
SIO_000300: 1.297126e6

MQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.545e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1228
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61214
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.450780544445878e-5
allele num: 15502
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.336e1

ClippingRankSum
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SIO_000300: -1.331e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQRankSum
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VQSLOD
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SIO_000300: 7.23e-1

MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.345007e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4168
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15522
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.211495946941784e-5
allele num: 10856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.256056264652253e-5
allele num: 61424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-2

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.383406e6

BaseQRankSum
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SIO_000300: -9.320000000000001e-1

MQRankSum
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FS
type: SiteQuality
SIO_000300: 1.559e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

GenotypeDepth
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variant carriers: 3495

GenotypeQuality
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variant carriers: 144

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1030
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GenotypeQuality
all individuals: 250
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GenotypeQuality
all individuals: 2754
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GenotypeQuality
all individuals: 813
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GenotypeQuality
all individuals: 1093
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variant carriers: 209

GenotypeQuality
all individuals: 364
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GenotypeQuality
all individuals: 2769
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variant carriers: 293

GenotypeQuality
all individuals: 186
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GenotypeQuality
all individuals: 436
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variant carriers: 159

GenotypeQuality
all individuals: 346
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variant carriers: 127

GenotypeQuality
all individuals: 19965
bin: 9.75e1
variant carriers: 18160

European (Finnish)
type: Population
allele count: 1067
allele frequency: 1.745175008177952e-1
allele num: 6114
num of homozygotes: 103

Other
type: Population
allele count: 179
allele frequency: 2.081395348837209e-1
allele num: 860
num of homozygotes: 24

South Asian
type: Population
allele count: 2312
allele frequency: 1.471861471861472e-1
allele num: 15708
num of homozygotes: 200

European (Non-Finnish)
type: Population
allele count: 17064
allele frequency: 2.724050956227451e-1
allele num: 62642
num of homozygotes: 2130

Latino
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allele count: 1113
allele frequency: 1.020539152759949e-1
allele num: 10906
num of homozygotes: 59

African
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allele count: 1152
allele frequency: 1.167173252279635e-1
allele num: 9870
num of homozygotes: 66

East Asian
type: Population
allele count: 6
allele frequency: 7.220216606498195e-4
allele num: 8310
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.776e1

ClippingRankSum
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SIO_000300: -4.12e-1

MQRankSum
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SIO_000300: 2.3e-2

ReadPosRankSum
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SIO_000300: 3.83e-1

VQSLOD
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SIO_000300: 6.47e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 3.98e-2

BaseQRankSum
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SIO_000300: 3.23e0

DP
type: SiteQuality
SIO_000300: 1.524375e6

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 868
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.571981010469394e-5
allele num: 63614
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9950
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15752
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11026
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6196
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

MQ
type: SiteQuality
SIO_000300: 5.837e1

FS
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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SIO_000300: 3.5e-3

QD
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SIO_000300: 1.402e1

BaseQRankSum
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SIO_000300: 2.45e0

ClippingRankSum
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SIO_000300: 4.12e-1

ReadPosRankSum
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SIO_000300: -3.15e-1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9962
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63720
num of homozygotes: 0

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

South Asian
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allele count: 29
allele frequency: 1.837769328263625e-3
allele num: 15780
num of homozygotes: 2

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11032
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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QD
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SIO_000300: 1.539e1

FS
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -5.7e-2

InbreedingCoeff
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SIO_000300: 1.81e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2164
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11054
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

South 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: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63738
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.004419445560466e-4
allele num: 9956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 2.95e0

ReadPosRankSum
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SIO_000300: 5.12e-1

MQRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.485749e6

QD
type: SiteQuality
SIO_000300: 1.314e1

FS
type: SiteQuality
SIO_000300: 1.925e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.137845555241771e-5
allele num: 63738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11054
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.34517766497462e-5
allele num: 15760
num of homozygotes: 0

VQSLOD
type: SiteQuality
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 1.925e0

InbreedingCoeff
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SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63858
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.001602564102564e-4
allele num: 9984
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15810
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.041591320072333e-5
allele num: 11060
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.612903225806452e-4
allele num: 6200
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.498085e6

BaseQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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SIO_000300: 6.0e1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.681647940074907e-5
allele num: 64080
num of homozygotes: 0

Other
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African
type: Population
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Latino
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South Asian
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East Asian
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DP
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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QD
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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)
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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African
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Other
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European (Non-Finnish)
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allele frequency: 3.114876650884625e-5
allele num: 64208
num of homozygotes: 0

FS
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.511528e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

QD
type: SiteQuality
SIO_000300: 1.629e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 149
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4839
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3059
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 393
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 879
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2355
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6252
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15864
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10044
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.058823529411765e-3
allele num: 8500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.9e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.112e0

FS
type: SiteQuality
SIO_000300: 2.41e0

DP
type: SiteQuality
SIO_000300: 1.525542e6

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-2

QD
type: SiteQuality
SIO_000300: 1.002e1

GenotypeDepth
all individuals: 16032
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1260
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4876
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11172
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.546312045770837e-5
allele num: 64670
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.897e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 3.144e0

VQSLOD
type: SiteQuality
SIO_000300: -3.953e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.459e0

DP
type: SiteQuality
SIO_000300: 1.533261e6

GenotypeDepth
all individuals: 122
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40324
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3056
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 553
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4876
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.944543828264758e-5
allele num: 11180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15904
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.296e0

VQSLOD
type: SiteQuality
SIO_000300: 4.78e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 3.047e0

MQRankSum
type: SiteQuality
SIO_000300: -6.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 1.535959e6

QD
type: SiteQuality
SIO_000300: 1.028e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.87e-1

GenotypeDepth
all individuals: 443
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1132
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3056
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4876
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40324
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 8
allele frequency: 7.155635062611807e-4
allele num: 11180
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15904
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.87e-1

DP
type: SiteQuality
SIO_000300: 1.535959e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: -6.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.78e-1

QD
type: SiteQuality
SIO_000300: 1.028e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 3.047e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.296e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.16e-1

GenotypeDepth
all individuals: 149
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3047
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 461
bin: 9.25e1
variant carriers: 0