9-108380241-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380241
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380241
    reference: chr 9
allele count: 1
allele frequency: 1.016921575008135e-5
allele num: 98336
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.912A>G
  hgvsp: ENST00000223528.2:c.912A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10009A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.912A>G
  hgvsp: ENST00000357998.5:c.912A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.912A>G
  hgvsp: ENST00000602661.1:c.912A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.912A>G
  hgvsp: ENST00000448551.2:c.912A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*950A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.2A>G
  hgvsp: ENST00000457847.1:c.2A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11075
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11137
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33763
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 7.75e1
  variant carriers: 0
hgvs: c.912A>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

9-108380241-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380241
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380241
    reference: chr 9
allele count: 1
allele frequency: 1.016921575008135e-5
allele num: 98336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.912A>T
  hgvsp: ENST00000602661.1:c.912A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.912A>T
  hgvsp: ENST00000223528.2:c.912A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.912A>T
  hgvsp: ENST00000448551.2:c.912A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10009A>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*950A>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.912A>T
  hgvsp: ENST00000357998.5:c.912A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.2A>T
  hgvsp: ENST00000457847.1:c.2A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11075
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3604
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 5.25e1
  variant carriers: 0
hgvs: c.912A>T
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

9-108380246-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380246
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380246
    reference: chr 9
allele count: 4
allele frequency: 3.918495297805643e-5
allele num: 102080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.917A>G
  hgvsp: ENSP00000473540.1:p.Tyr306Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*955A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.7A>G
  hgvsp: ENSP00000414114.1:p.Tyr3Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.917A>G
  hgvsp: ENSP00000223528.2:p.Tyr306Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.917A>G
  hgvsp: ENSP00000350687.5:p.Tyr306Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.917A>G
  hgvsp: ENSP00000399140.2:p.Tyr306Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10014A>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6220
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36264
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9445
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Tyr306Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

9-108380248-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380248
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380248
    reference: chr 9
allele count: 1
allele frequency: 9.68710646130001e-6
allele num: 103230
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*957C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.919C>T
  hgvsp: ENSP00000399140.2:p.Arg307Ter
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.919C>T
  hgvsp: ENSP00000223528.2:p.Arg307Ter
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.9C>T
  hgvsp: ENSP00000414114.1:p.Arg4Ter
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.919C>T
  hgvsp: ENSP00000350687.5:p.Arg307Ter
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10016C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: stop_gained
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.919C>T
  hgvsp: ENSP00000473540.1:p.Arg307Ter
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36630
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg307Ter
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS

9-108380250-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380250
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380250
    reference: chr 9
allele count: 1
allele frequency: 9.525079534414112e-6
allele num: 104986
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.921A>G
  hgvsp: ENST00000223528.2:c.921A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.921A>G
  hgvsp: ENST00000602661.1:c.921A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.11A>G
  hgvsp: ENST00000457847.1:c.11A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*959A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.921A>G
  hgvsp: ENST00000357998.5:c.921A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.921A>G
  hgvsp: ENST00000448551.2:c.921A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10018A>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8064
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg307Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-108380254-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380254
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380254
    reference: chr 9
allele count: 1
allele frequency: 9.330969487729775e-6
allele num: 107170
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10022T>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.925T>G
  hgvsp: ENSP00000223528.2:p.Cys309Gly
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.925T>G
  hgvsp: ENSP00000350687.5:p.Cys309Gly
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.925T>G
  hgvsp: ENSP00000399140.2:p.Cys309Gly
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.925T>G
  hgvsp: ENSP00000473540.1:p.Cys309Gly
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.15T>G
  hgvsp: ENSP00000414114.1:p.Cys6Gly
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*963T>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6918
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3262
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7045
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys309Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-108380258-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380258
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380258
    reference: chr 9
allele count: 6
allele frequency: 5.509338328466751e-5
allele num: 108906
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10026A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.19A>G
  hgvsp: ENSP00000414114.1:p.Asn7Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*967A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.929A>G
  hgvsp: ENSP00000350687.5:p.Asn310Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.929A>G
  hgvsp: ENSP00000223528.2:p.Asn310Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.929A>G
  hgvsp: ENSP00000473540.1:p.Asn310Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.929A>G
  hgvsp: ENSP00000399140.2:p.Asn310Ser
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3268
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn310Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS

9-108380281-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380281
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380281
    reference: chr 9
allele count: 2
allele frequency: 1.750730930163343e-5
allele num: 114238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*990G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.952G>A
  hgvsp: ENSP00000223528.2:p.Val318Ile
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.952G>A
  hgvsp: ENSP00000350687.5:p.Val318Ile
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10049G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.952G>A
  hgvsp: ENSP00000473540.1:p.Val318Ile
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.952G>A
  hgvsp: ENSP00000399140.2:p.Val318Ile
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.42G>A
  hgvsp: ENSP00000414114.1:p.Val15Ile
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39733
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val318Ile
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

9-108380301-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380301
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380301
    reference: chr 9
allele count: 1
allele frequency: 8.59017970655946e-6
allele num: 116412
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.972A>G
  hgvsp: ENSP00000223528.2:p.Ile324Met
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1010A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.972A>G
  hgvsp: ENSP00000473540.1:p.Ile324Met
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.62A>G
  hgvsp: ENSP00000414114.1:p.Ile21Met
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.972A>G
  hgvsp: ENSP00000399140.2:p.Ile324Met
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.972A>G
  hgvsp: ENSP00000350687.5:p.Ile324Met
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10069A>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9848
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4680
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1898
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38495
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile324Met
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/9-108380304-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380304
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380304
    reference: chr 9
allele count: 1
allele frequency: 8.566484486096596e-6
allele num: 116734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1013A>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.975A>C
  hgvsp: ENSP00000399140.2:p.Gln325His
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.975A>C
  hgvsp: ENSP00000473540.1:p.Gln325His
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.975A>C
  hgvsp: ENSP00000223528.2:p.Gln325His
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.65A>C
  hgvsp: ENSP00000414114.1:p.Gln22His
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.975A>C
  hgvsp: ENSP00000350687.5:p.Gln325His
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10072A>C
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1921
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4727
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln325His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

9-108380306-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380306
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380306
    reference: chr 9
allele count: 1
allele frequency: 8.550370231031004e-6
allele num: 116954
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.67A>G
  hgvsp: ENSP00000414114.1:p.Asp23Gly
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.977A>G
  hgvsp: ENSP00000399140.2:p.Asp326Gly
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1015A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.977A>G
  hgvsp: ENSP00000223528.2:p.Asp326Gly
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.977A>G
  hgvsp: ENSP00000350687.5:p.Asp326Gly
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.977A>G
  hgvsp: ENSP00000473540.1:p.Asp326Gly
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10074A>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39547
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1929
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4757
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp326Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

9-108380309-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380309
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380309
    reference: chr 9
allele count: 1
allele frequency: 8.534462158194791e-6
allele num: 117172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1018A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.70A>G
  hgvsp: ENSP00000414114.1:p.Tyr24Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10077A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.980A>G
  hgvsp: ENSP00000399140.2:p.Tyr327Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.980A>G
  hgvsp: ENSP00000473540.1:p.Tyr327Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.980A>G
  hgvsp: ENSP00000223528.2:p.Tyr327Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.980A>G
  hgvsp: ENSP00000350687.5:p.Tyr327Cys
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1438
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39690
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr327Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

9-108380338-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380338
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380338
    reference: chr 9
allele count: 2
allele frequency: 1.672744304305644e-5
allele num: 119564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1009G>T
  hgvsp: ENSP00000473540.1:p.Asp337Tyr
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1047G>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.99G>T
  hgvsp: ENSP00000414114.1:p.Asp34Tyr
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1009G>T
  hgvsp: ENSP00000223528.2:p.Asp337Tyr
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1009G>T
  hgvsp: ENSP00000399140.2:p.Asp337Tyr
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1009G>T
  hgvsp: ENSP00000350687.5:p.Asp337Tyr
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10106G>T
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5193
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1829
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp337Tyr
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

9-108380339-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380339
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380339
    reference: chr 9
allele count: 1
allele frequency: 8.359386755387625e-6
allele num: 119626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1010A>T
  hgvsp: ENSP00000350687.5:p.Asp337Val
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1010A>T
  hgvsp: ENSP00000473540.1:p.Asp337Val
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.100A>T
  hgvsp: ENSP00000414114.1:p.Asp34Val
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1010A>T
  hgvsp: ENSP00000399140.2:p.Asp337Val
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1048A>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1010A>T
  hgvsp: ENSP00000223528.2:p.Asp337Val
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10107A>T
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1598
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp337Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

9-108380351-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380351
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380351
    reference: chr 9
allele count: 1
allele frequency: 8.342092530490349e-6
allele num: 119874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1022C>T
  hgvsp: ENSP00000473540.1:p.Pro341Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1060C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1022C>T
  hgvsp: ENSP00000350687.5:p.Pro341Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10119C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1022C>T
  hgvsp: ENSP00000399140.2:p.Pro341Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1022C>T
  hgvsp: ENSP00000223528.2:p.Pro341Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.112C>T
  hgvsp: ENSP00000414114.1:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3351
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42176
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro341Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

9-108380352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380352
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380352
    reference: chr 9
allele count: 105
allele frequency: 8.758466517633712e-4
allele num: 119884
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.113G>A
  hgvsp: ENST00000457847.1:c.113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1023G>A
  hgvsp: ENST00000448551.2:c.1023G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1023G>A
  hgvsp: ENST00000357998.5:c.1023G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1061G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1023G>A
  hgvsp: ENST00000223528.2:c.1023G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10120G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1023G>A
  hgvsp: ENST00000602661.1:c.1023G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11526
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 39609
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5228
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro341Pro
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

9-108380352-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380352
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380352
    reference: chr 9
allele count: 2
allele frequency: 1.668279336692136e-5
allele num: 119884
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1061G>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1023G>T
  hgvsp: ENST00000602661.1:c.1023G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1023G>T
  hgvsp: ENST00000448551.2:c.1023G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1023G>T
  hgvsp: ENST00000223528.2:c.1023G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10120G>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1023G>T
  hgvsp: ENST00000357998.5:c.1023G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.113G>T
  hgvsp: ENST00000457847.1:c.113G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5228
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42169
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro341Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/9-108380355-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380355
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380355
    reference: chr 9
allele count: 30276
allele frequency: 2.518466759832302e-1
allele num: 120216
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10123C>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1026C>A
  hgvsp: ENST00000448551.2:c.1026C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1064C>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1026C>A
  hgvsp: ENST00000602661.1:c.1026C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.116C>A
  hgvsp: ENST00000457847.1:c.116C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  clinical significance: benign&likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1026C>A
  hgvsp: ENST00000223528.2:c.1026C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1026C>A
  hgvsp: ENST00000357998.5:c.1026C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 568
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 5.75e1
  variant carriers: 1745
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.75e1
  variant carriers: 474
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 447
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 3.25e1
  variant carriers: 2641
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.5e0
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 4.75e1
  variant carriers: 2820
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.75e1
  variant carriers: 248
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 2.75e1
  variant carriers: 2049
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 6.25e1
  variant carriers: 1294
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 3.75e1
  variant carriers: 3007
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 8.25e1
  variant carriers: 357
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.25e1
  variant carriers: 244
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 6.75e1
  variant carriers: 890
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 4.25e1
  variant carriers: 3147
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 9.75e1
  variant carriers: 2545
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 5.25e1
  variant carriers: 2257
genotype depth: GenotypeDepth
  all individuals: 23780
  bin: 2.25e1
  variant carriers: 1175
genotype quality: GenotypeQuality
  all individuals: 2699
  bin: 6.75e1
  variant carriers: 150
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.25e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 9.25e1
  variant carriers: 180
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 2.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 7.75e1
  variant carriers: 155
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 9
hgvs: p.Leu342Leu
num of homozygotes: 4258
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

9-108380366-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380366
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380366
    reference: chr 9
allele count: 2
allele frequency: 1.666055779547499e-5
allele num: 120044
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1037T>C
  hgvsp: ENSP00000223528.2:p.Phe346Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10134T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1037T>C
  hgvsp: ENSP00000473540.1:p.Phe346Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1037T>C
  hgvsp: ENSP00000399140.2:p.Phe346Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1037T>C
  hgvsp: ENSP00000350687.5:p.Phe346Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.127T>C
  hgvsp: ENSP00000414114.1:p.Phe43Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1075T>C
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2060
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1831
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe346Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD

9-108380390-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380390
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380390
    reference: chr 9
allele count: 3
allele frequency: 2.511721366376423e-5
allele num: 119440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1082+17G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.134+17G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1044+17G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10158G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1044+17G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1044+17G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1044+17G>A
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6704
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6103
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2478
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1846
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-108380390-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380390
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380390
    reference: chr 9
allele count: 1
allele frequency: 8.372404554588077e-6
allele num: 119440
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10158G>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1082+17G>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1044+17G>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.134+17G>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1044+17G>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1044+17G>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1044+17G>C
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36196
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1917
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6103
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 3.25e1
  variant carriers: 0
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: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP

9-108380397-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380397
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380397
    reference: chr 9
allele count: 1
allele frequency: 8.381948635418762e-6
allele num: 119304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1044+24T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1044+24T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1044+24T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1044+24T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1082+24T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10165T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.134+24T>C
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34132
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

9-108380401-ATAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380401
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380397
    reference: chr 9
allele count: 1
allele frequency: 8.391655337931961e-6
allele num: 119166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10173_780+10176delGTAA
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1044+32_1044+35delGTAA
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1044+32_1044+35delGTAA
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1044+32_1044+35delGTAA
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.134+32_134+35delGTAA
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1082+32_*1082+35delGTAA
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1044+32_1044+35delGTAA
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4856
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2355
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: ATAAG
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

9-108380410-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380410
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380410
    reference: chr 9
allele count: 1
allele frequency: 8.411419342899921e-6
allele num: 118886
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1044+37A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10178A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1044+37A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1082+37A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1044+37A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.134+37A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1044+37A>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7041
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21562
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6094
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1676
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-108380411-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380411
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380411
    reference: chr 9
allele count: 1
allele frequency: 8.413825598223e-6
allele num: 118852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1044+38T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1044+38T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.134+38T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1082+38T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1044+38T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1044+38T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10179T>C
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1731
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1454
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2290
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

9-108380416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380416
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380416
    reference: chr 9
allele count: 1
allele frequency: 8.432983083435934e-6
allele num: 118582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1082+43C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1044+43C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.134+43C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1044+43C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10184C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1044+43C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1044+43C>T
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11031
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2238
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2082
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6094
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1601
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

9-108380417-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380417
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380417
    reference: chr 9
allele count: 3222
allele frequency: 2.718161571168253e-2
allele num: 118536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.134+44A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1082+44A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1044+44A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1044+44A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1044+44A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10185A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1044+44A>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 10767
  bin: 2.75e1
  variant carriers: 620
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 1.25e1
  variant carriers: 184
genotype depth: GenotypeDepth
  all individuals: 9169
  bin: 1.75e1
  variant carriers: 439
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 7.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 3.25e1
  variant carriers: 429
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 21538
  bin: 2.25e1
  variant carriers: 617
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 4.25e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 3.75e1
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 9.75e1
  variant carriers: 160
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1195
  bin: 5.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 4201
  bin: 6.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 4.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3184
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2990
  bin: 4.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2475
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 8.75e1
  variant carriers: 8
num of homozygotes: 55
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

9-108380419-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108380419
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108380419
    reference: chr 9
allele count: 1
allele frequency: 8.449371366770313e-6
allele num: 118352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.134+46T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1082+46T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1044+46T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1044+46T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1044+46T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+10187T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1044+46T>C
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2519
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4581
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1697
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4425
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4242
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1601
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/9-108382175-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382175
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382175
    reference: chr 9
allele count: 431
allele frequency: 3.979906550686095e-3
allele num: 108294
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1045-40C>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1045-40C>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1045-40C>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.135-40C>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+11943C>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1045-40C>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1083-40C>A
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 25402
  bin: 2.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6113
  bin: 2.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9161
  bin: 1.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 1.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 3.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2198
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3339
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24446
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5214
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4269
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 1
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

9-108382187-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382187
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382187
    reference: chr 9
allele count: 2
allele frequency: 1.756789993324198e-5
allele num: 113844
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1045-28T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1045-28T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1083-28T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1045-28T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1045-28T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+11955T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.135-28T>C
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7452
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4891
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3422
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7689
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

9-108382188-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382188
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382188
    reference: chr 9
allele count: 1
allele frequency: 8.761477535571598e-6
allele num: 114136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1083-27G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1045-27G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1045-27G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.135-27G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+11956G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1045-27G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1045-27G>A
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4950
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3285
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

9-108382192-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382192
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382192
    reference: chr 9
allele count: 1
allele frequency: 8.665060742075802e-6
allele num: 115406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1045-23G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1045-23G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.135-23G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+11960G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1045-23G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1045-23G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1083-23G>A
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

9-108382193-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382193
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382193
    reference: chr 9
allele count: 1
allele frequency: 8.638562543192813e-6
allele num: 115760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1045-22A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1045-22A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1045-22A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1083-22A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1045-22A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+11961A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.135-22A>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36243
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5098
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

9-108382209-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382209
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382209
    reference: chr 9
allele count: 1
allele frequency: 8.440100605999223e-6
allele num: 118482
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1045-6C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+11977C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1045-6C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1083-6C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1045-6C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.135-6C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1045-6C>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9042
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2064
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 907
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1045-6C>G
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

9-108382212-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382212
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382212
    reference: chr 9
allele count: 1
allele frequency: 8.415949908266146e-6
allele num: 118822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.135-3T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+11980T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1045-3T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1045-3T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1045-3T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1083-3T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1045-3T>C
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1446
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2076
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38350
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1045-3T>C
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

9-108382216-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382216
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382216
    reference: chr 9
allele count: 1
allele frequency: 8.39602364320258e-6
allele num: 119104
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1046T>C
  hgvsp: ENSP00000350687.5:p.Val349Ala
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1046T>C
  hgvsp: ENSP00000223528.2:p.Val349Ala
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1046T>C
  hgvsp: ENSP00000399140.2:p.Val349Ala
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.136T>C
  hgvsp: ENSP00000414114.1:p.Val46Ala
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1084T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+11984T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1046T>C
  hgvsp: ENSP00000473540.1:p.Val349Ala
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 909
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val349Ala
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

9-108382218-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382218
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382218
    reference: chr 9
allele count: 1
allele frequency: 8.387713677005921e-6
allele num: 119222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1048G>A
  hgvsp: ENSP00000473540.1:p.Glu350Lys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1048G>A
  hgvsp: ENSP00000223528.2:p.Glu350Lys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.138G>A
  hgvsp: ENSP00000414114.1:p.Glu47Lys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+11986G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1048G>A
  hgvsp: ENSP00000350687.5:p.Glu350Lys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1048G>A
  hgvsp: ENSP00000399140.2:p.Glu350Lys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1086G>A
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9483
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7692
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu350Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/9-108382224-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382224
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382224
    reference: chr 9
allele count: 1
allele frequency: 8.36988181726874e-6
allele num: 119476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1092A>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+11992A>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.144A>C
  hgvsp: ENSP00000414114.1:p.Ser49Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1054A>C
  hgvsp: ENSP00000399140.2:p.Ser352Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1054A>C
  hgvsp: ENSP00000350687.5:p.Ser352Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1054A>C
  hgvsp: ENSP00000223528.2:p.Ser352Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1054A>C
  hgvsp: ENSP00000473540.1:p.Ser352Arg
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37006
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2063
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38490
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5383
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser352Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

9-108382226-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382226
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382226
    reference: chr 9
allele count: 3
allele frequency: 2.509116456458466e-5
allele num: 119564
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1056C>G
  hgvsp: ENSP00000350687.5:p.Ser352Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1056C>G
  hgvsp: ENSP00000399140.2:p.Ser352Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1056C>G
  hgvsp: ENSP00000223528.2:p.Ser352Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1056C>G
  hgvsp: ENSP00000473540.1:p.Ser352Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.146C>G
  hgvsp: ENSP00000414114.1:p.Ser49Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+11994C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1094C>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1449
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7694
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser352Arg
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

9-108382235-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382235
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382235
    reference: chr 9
allele count: 1
allele frequency: 8.345155637152633e-6
allele num: 119830
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1065A>G
  hgvsp: ENST00000357998.5:c.1065A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.155A>G
  hgvsp: ENST00000457847.1:c.155A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1103A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1065A>G
  hgvsp: ENST00000448551.2:c.1065A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12003A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1065A>G
  hgvsp: ENST00000223528.2:c.1065A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1065A>G
  hgvsp: ENST00000602661.1:c.1065A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2061
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1757
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7692
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu355Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

9-108382269-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382269
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382268
    reference: chr 9
allele count: 2
allele frequency: 1.660164356271271e-5
allele num: 120470
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1106delT
  hgvsp: ENSP00000223528.2:p.Phe369SerfsTer37
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1106delT
  hgvsp: ENSP00000399140.2:p.Phe369SerfsTer37
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1144delT
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1106delT
  hgvsp: ENSP00000473540.1:p.Phe369SerfsTer37
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1106delT
  hgvsp: ENSP00000350687.5:p.Phe369SerfsTer37
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.196delT
  hgvsp: ENSP00000414114.1:p.Phe66SerfsTer37
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12044delT
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe369SerfsTer37
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: GT
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

9-108382272-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382272
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382272
    reference: chr 9
allele count: 3
allele frequency: 2.489213408562894e-5
allele num: 120520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.192T>C
  hgvsp: ENSP00000414114.1:p.Phe65Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1102T>C
  hgvsp: ENSP00000473540.1:p.Phe368Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12040T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1102T>C
  hgvsp: ENSP00000399140.2:p.Phe368Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1140T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1102T>C
  hgvsp: ENSP00000223528.2:p.Phe368Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1102T>C
  hgvsp: ENSP00000350687.5:p.Phe368Leu
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38913
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7694
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Phe368Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

9-108382276-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382276
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382276
    reference: chr 9
allele count: 1
allele frequency: 8.29462508294625e-6
allele num: 120560
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.196T>C
  hgvsp: ENSP00000414114.1:p.Phe66Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1106T>C
  hgvsp: ENSP00000473540.1:p.Phe369Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1106T>C
  hgvsp: ENSP00000399140.2:p.Phe369Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1106T>C
  hgvsp: ENSP00000223528.2:p.Phe369Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1106T>C
  hgvsp: ENSP00000350687.5:p.Phe369Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12044T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1144T>C
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5517
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe369Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

9-108382280-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382280
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382280
    reference: chr 9
allele count: 1
allele frequency: 8.29132395860971e-6
allele num: 120608
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1110C>T
  hgvsp: ENST00000223528.2:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1110C>T
  hgvsp: ENST00000448551.2:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1110C>T
  hgvsp: ENST00000357998.5:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1148C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1110C>T
  hgvsp: ENST00000602661.1:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.200C>T
  hgvsp: ENST00000457847.1:c.200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12048C>T
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe370Phe
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

9-108382282-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382282
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382282
    reference: chr 9
allele count: 3
allele frequency: 2.486613729423271e-5
allele num: 120646
alternate allele: G
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12050A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1112A>G
  hgvsp: ENSP00000399140.2:p.Tyr371Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.202A>G
  hgvsp: ENSP00000414114.1:p.Tyr68Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1150A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1112A>G
  hgvsp: ENSP00000350687.5:p.Tyr371Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1112A>G
  hgvsp: ENSP00000473540.1:p.Tyr371Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  clinical significance: pathogenic
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1112A>G
  hgvsp: ENSP00000223528.2:p.Tyr371Cys
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7693
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5529
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr371Cys
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/9-108382289-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382289
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382289
    reference: chr 9
allele count: 1
allele frequency: 8.285827919925758e-6
allele num: 120688
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1119A>C
  hgvsp: ENSP00000223528.2:p.Glu373Asp
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1119A>C
  hgvsp: ENSP00000473540.1:p.Glu373Asp
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1119A>C
  hgvsp: ENSP00000350687.5:p.Glu373Asp
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.209A>C
  hgvsp: ENSP00000414114.1:p.Glu70Asp
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1157A>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12057A>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1119A>C
  hgvsp: ENSP00000399140.2:p.Glu373Asp
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39622
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu373Asp
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

9-108382293-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382293
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382293
    reference: chr 9
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1123G>A
  hgvsp: ENSP00000399140.2:p.Asp375Asn
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1123G>A
  hgvsp: ENSP00000350687.5:p.Asp375Asn
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1161G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1123G>A
  hgvsp: ENSP00000223528.2:p.Asp375Asn
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12061G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1123G>A
  hgvsp: ENSP00000473540.1:p.Asp375Asn
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.213G>A
  hgvsp: ENSP00000414114.1:p.Asp72Asn
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39657
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp375Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/9-108382313-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382313
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382313
    reference: chr 9
allele count: 1
allele frequency: 8.298755186721992e-6
allele num: 120500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1181C>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.233C>A
  hgvsp: ENST00000457847.1:c.233C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1143C>A
  hgvsp: ENST00000448551.2:c.1143C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12081C>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1143C>A
  hgvsp: ENST00000223528.2:c.1143C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1143C>A
  hgvsp: ENST00000602661.1:c.1143C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1143C>A
  hgvsp: ENST00000357998.5:c.1143C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2073
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7692
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5493
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly381Gly
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

9-108382329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382329
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382329
    reference: chr 9
allele count: 55
allele frequency: 4.577154175196818e-4
allele num: 120162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12097G>A
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1159G>A
  hgvsp: ENSP00000350687.5:p.Gly387Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1159G>A
  hgvsp: ENSP00000473540.1:p.Gly387Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1159G>A
  hgvsp: ENSP00000223528.2:p.Gly387Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.249G>A
  hgvsp: ENSP00000414114.1:p.Gly84Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1159G>A
  hgvsp: ENSP00000399140.2:p.Gly387Arg
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1197G>A
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35049
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11953
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2047
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly387Arg
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

9-108382330-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382330
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382331
    reference: chr 9
allele count: 34
allele frequency: 2.830738489717759e-4
allele num: 120110
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12105dupA
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1167dupA
  hgvsp: ENSP00000223528.2:p.Phe390IlefsTer14
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1167dupA
  hgvsp: ENSP00000399140.2:p.Phe390IlefsTer14
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.257dupA
  hgvsp: ENSP00000414114.1:p.Phe87IlefsTer14
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1205dupA
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1167dupA
  hgvsp: ENSP00000350687.5:p.Phe390IlefsTer14
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1167dupA
  hgvsp: ENSP00000473540.1:p.Phe390IlefsTer14
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11960
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34970
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5400
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7707
  bin: 9.75e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe390IlefsTer14
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

9-108382339-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382339
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382339
    reference: chr 9
allele count: 1
allele frequency: 8.343484572897024e-6
allele num: 119854
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.259T>G
  hgvsp: ENSP00000414114.1:p.Phe87Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1169T>G
  hgvsp: ENSP00000399140.2:p.Phe390Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12107T>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1169T>G
  hgvsp: ENSP00000350687.5:p.Phe390Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1169T>G
  hgvsp: ENSP00000473540.1:p.Phe390Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1169T>G
  hgvsp: ENSP00000223528.2:p.Phe390Cys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1207T>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe390Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

9-108382355-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382355
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382355
    reference: chr 9
allele count: 81
allele frequency: 6.809812856254098e-4
allele num: 118946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.262+13T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1210+13T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12123T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1172+13T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1172+13T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1172+13T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1172+13T>C
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11230
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 32585
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1879
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

9-108382357-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382357
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382357
    reference: chr 9
allele count: 1
allele frequency: 8.411843876177658e-6
allele num: 118880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1172+15A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1172+15A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1172+15A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1210+15A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.262+15A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12125A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1172+15A>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11200
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7694
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

9-108382385-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382385
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382385
    reference: chr 9
allele count: 1
allele frequency: 8.490405841399219e-6
allele num: 117780
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1172+43A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1172+43A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1210+43A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12153A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1172+43A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1172+43A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.262+43A>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3015
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3748
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2410
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7694
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

9-108382392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108382392
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108382392
    reference: chr 9
allele count: 1
allele frequency: 8.538542983025377e-6
allele num: 117116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1172+50C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1172+50C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.780+12160C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1172+50C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1172+50C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1210+50C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.262+50C>T
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9055
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7691
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2062
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1557
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4932
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3147
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4114
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

9-108397289-CCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397289
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397286
    reference: chr 9
allele count: 4
allele frequency: 3.299622193258872e-5
allele num: 121226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1173-38_1173-36delTTC
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1173-38_1173-36delTTC
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1173-38_1173-36delTTC
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1173-38_1173-36delTTC
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.781-38_781-36delTTC
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1211-38_*1211-36delTTC
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.263-38_263-36delTTC
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3322
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: CCTT
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

9-108397290-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397290
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397290
    reference: chr 9
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1173-42C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1173-42C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.781-42C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1173-42C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.263-42C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1211-42C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1173-42C>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25520
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4384
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3317
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

9-108397290-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397290
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397290
    reference: chr 9
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1173-42C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1173-42C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1211-42C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.781-42C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.263-42C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1173-42C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1173-42C>T
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16604
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10899
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3155
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25520
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

9-108397297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397297
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397297
    reference: chr 9
allele count: 3
allele frequency: 2.473777953690877e-5
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1173-35C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.263-35C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.781-35C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1173-35C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1211-35C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1173-35C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1173-35C>T
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25885
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10902
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4379
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

9-108397298-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397298
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397298
    reference: chr 9
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1173-34A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1173-34A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1173-34A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1173-34A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.781-34A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1211-34A>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.263-34A>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4379
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8999
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

9-108397318-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397318
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397318
    reference: chr 9
allele count: 2
allele frequency: 1.648125257519571e-5
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.781-14C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1173-14C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1173-14C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1211-14C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.263-14C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1173-14C>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1173-14C>G
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3315
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4374
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

9-108397324-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397324
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397324
    reference: chr 9
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1173-8T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1173-8T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.781-8T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1211-8T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1173-8T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1173-8T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.263-8T>C
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7770
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4373
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26168
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10899
  bin: 9.75e1
  variant carriers: 2
hgvs: c.1173-8T>C
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

9-108397333-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397333
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397333
    reference: chr 9
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1174T>C
  hgvsp: ENSP00000350687.5:p.Tyr392His
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1174T>C
  hgvsp: ENSP00000473540.1:p.Tyr392His
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1174T>C
  hgvsp: ENSP00000399140.2:p.Tyr392His
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.782T>C
  hgvsp: ENSP00000439423.1:p.Ile261Thr
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1212T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1174T>C
  hgvsp: ENSP00000223528.2:p.Tyr392His
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.264T>C
  hgvsp: ENSP00000414114.1:p.Tyr89His
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2249
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr392His
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

9-108397337-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397337
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397337
    reference: chr 9
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1178T>C
  hgvsp: ENSP00000399140.2:p.Leu393Pro
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1216T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.268T>C
  hgvsp: ENSP00000414114.1:p.Leu90Pro
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1178T>C
  hgvsp: ENSP00000350687.5:p.Leu393Pro
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1178T>C
  hgvsp: ENSP00000223528.2:p.Leu393Pro
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.786T>C
  hgvsp: ENST00000540160.1:c.786T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1178T>C
  hgvsp: ENSP00000473540.1:p.Leu393Pro
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4374
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10898
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3143
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu393Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

9-108397338-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397338
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397338
    reference: chr 9
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.269G>C
  hgvsp: ENST00000457847.1:c.269G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1179G>C
  hgvsp: ENST00000448551.2:c.1179G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1217G>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1179G>C
  hgvsp: ENST00000223528.2:c.1179G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1179G>C
  hgvsp: ENST00000602661.1:c.1179G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.787G>C
  hgvsp: ENSP00000439423.1:p.Val263Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1179G>C
  hgvsp: ENST00000357998.5:c.1179G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10896
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3143
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2248
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val263Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

9-108397340-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397340
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397340
    reference: chr 9
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1181T>C
  hgvsp: ENSP00000473540.1:p.Phe394Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1181T>C
  hgvsp: ENSP00000399140.2:p.Phe394Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.789T>C
  hgvsp: ENST00000540160.1:c.789T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1181T>C
  hgvsp: ENSP00000350687.5:p.Phe394Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1219T>C
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.271T>C
  hgvsp: ENSP00000414114.1:p.Phe91Ser
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1181T>C
  hgvsp: ENSP00000223528.2:p.Phe394Ser
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4376
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2248
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe394Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

9-108397341-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397341
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397341
    reference: chr 9
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1182T>G
  hgvsp: ENSP00000350687.5:p.Phe394Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1182T>G
  hgvsp: ENSP00000399140.2:p.Phe394Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1220T>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1182T>G
  hgvsp: ENSP00000223528.2:p.Phe394Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1182T>G
  hgvsp: ENSP00000473540.1:p.Phe394Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.272T>G
  hgvsp: ENSP00000414114.1:p.Phe91Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.790T>G
  hgvsp: ENSP00000439423.1:p.Ser264Ala
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16673
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9014
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4377
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10895
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Phe394Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-108397344-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397344
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397344
    reference: chr 9
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.793G>A
  hgvsp: ENSP00000439423.1:p.Glu265Lys
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1185G>A
  hgvsp: ENST00000448551.2:c.1185G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1185G>A
  hgvsp: ENST00000357998.5:c.1185G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.275G>A
  hgvsp: ENST00000457847.1:c.275G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1185G>A
  hgvsp: ENST00000602661.1:c.1185G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1185G>A
  hgvsp: ENST00000223528.2:c.1185G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1223G>A
  variant of: http://identifiers.org/hgnc/3622
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4376
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10895
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26202
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu265Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

9-108397344-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397344
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397344
    reference: chr 9
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1185G>T
  hgvsp: ENST00000357998.5:c.1185G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1185G>T
  hgvsp: ENST00000223528.2:c.1185G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1185G>T
  hgvsp: ENST00000602661.1:c.1185G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1223G>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.793G>T
  hgvsp: ENSP00000439423.1:p.Glu265Ter
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1185G>T
  hgvsp: ENST00000448551.2:c.1185G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.275G>T
  hgvsp: ENST00000457847.1:c.275G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9016
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4376
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10895
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Glu265Ter
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

9-108397354-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397354
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397354
    reference: chr 9
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1233C>T
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1195C>T
  hgvsp: ENST00000602661.1:c.1195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.285C>T
  hgvsp: ENST00000457847.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1195C>T
  hgvsp: ENST00000223528.2:c.1195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1195C>T
  hgvsp: ENST00000357998.5:c.1195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1195C>T
  hgvsp: ENST00000448551.2:c.1195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.803C>T
  hgvsp: ENSP00000439423.1:p.Thr268Ile
  variant of: http://identifiers.org/hgnc/3622
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10891
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr268Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

9-108397367-AGTTTGTAGACATGAAGGTCCATGTACCCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397367
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397338
    reference: chr 9
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsp: ENSP00000399140.2:p.Phe404Ter
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsp: ENSP00000473540.1:p.Phe404Ter
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsp: ENSP00000414114.1:p.Phe101Ter
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsp: ENSP00000350687.5:p.Phe404Ter
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsp: ENSP00000223528.2:p.Phe404Ter
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 17963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26213
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4375
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe404Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: AGTTTGTAGACATGAAGGTCCATGTACCCT
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

9-108397371-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 108397371
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 108397371
    reference: chr 9
allele count: 7
allele frequency: 5.765872623636783e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473540
  ensembl transcript: ENST00000602661
  gene symbol: FKTN
  hgvsc: ENST00000602661.1:c.1212T>G
  hgvsp: ENSP00000473540.1:p.Phe404Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000473347
  ensembl transcript: ENST00000602526
  gene symbol: FKTN
  hgvsc: ENST00000602526.1:c.*1250T>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000439423
  ensembl transcript: ENST00000540160
  gene symbol: FKTN
  hgvsc: ENST00000540160.1:c.*4T>G
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000399140
  ensembl transcript: ENST00000448551
  gene symbol: FKTN
  hgvsc: ENST00000448551.2:c.1212T>G
  hgvsp: ENSP00000399140.2:p.Phe404Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000350687
  ensembl transcript: ENST00000357998
  gene symbol: FKTN
  hgvsc: ENST00000357998.5:c.1212T>G
  hgvsp: ENSP00000350687.5:p.Phe404Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000414114
  ensembl transcript: ENST00000457847
  gene symbol: FKTN
  hgvsc: ENST00000457847.1:c.302T>G
  hgvsp: ENSP00000414114.1:p.Phe101Leu
  variant of: http://identifiers.org/hgnc/3622
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106692
  ensembl protein: ENSP00000223528
  ensembl transcript: ENST00000223528
  gene symbol: FKTN
  hgvsc: ENST00000223528.2:c.1212T>G
  hgvsp: ENSP00000223528.2:p.Phe404Leu
  variant of: http://identifiers.org/hgnc/3622
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Phe404Leu
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 359
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.75e1
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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 51932
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.924248719013987e-5
allele num: 14442
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

MQ
type: SiteQuality
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VQSLOD
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SIO_000300: -5.159e-1

QD
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SIO_000300: 9.199999999999999e0

ClippingRankSum
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SIO_000300: 3.67e-1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 7.341e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7462
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.925595008857737e-5
allele num: 51932
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.341e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.67e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.312259e6

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: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 7.365668618568851e-5
allele num: 54306
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5988
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14786
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-1

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.68e-1

FS
type: SiteQuality
SIO_000300: 3.816e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.73e-1

DP
type: SiteQuality
SIO_000300: 1.345875e6

QD
type: SiteQuality
SIO_000300: 1.279e1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14838
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10562
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.815672888372431e-5
allele num: 55076
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 4.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.263e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQRankSum
type: SiteQuality
SIO_000300: -5.44e-1

DP
type: SiteQuality
SIO_000300: 1.358158e6

VQSLOD
type: SiteQuality
SIO_000300: -1.995e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8008
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15004
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10658
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.779232794818874e-5
allele num: 56204
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.929e1

DP
type: SiteQuality
SIO_000300: 1.372942e6

FS
type: SiteQuality
SIO_000300: 1.1293e1

VQSLOD
type: SiteQuality
SIO_000300: -1.474e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

QD
type: SiteQuality
SIO_000300: 1.384e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.373e0

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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.736231682755747e-5
allele num: 57596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10768
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8156
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.39224e6

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.901e0

QD
type: SiteQuality
SIO_000300: 3.328e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.83e-1

ReadPosRankSum
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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variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.586294416243655e-4
allele num: 6304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 5
allele frequency: 8.517307168165713e-5
allele num: 58704
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.98e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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QD
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.262466860244918e-4
allele num: 15842
num of homozygotes: 0

Other
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: 9236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.001e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.01e0

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

DP
type: SiteQuality
SIO_000300: 1.460609e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63616
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6514
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African
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allele count: 1
allele frequency: 1.047998323202683e-4
allele num: 9542
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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MQ
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ClippingRankSum
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FS
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 789
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56710336613803e-5
allele num: 63812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16044
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.82e-1

DP
type: SiteQuality
SIO_000300: 1.491076e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

QD
type: SiteQuality
SIO_000300: 8.970000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeQuality
all individuals: 564
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3279
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 843
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16072
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563574957783476e-5
allele num: 63956
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.493388e6

FS
type: SiteQuality
SIO_000300: 4.773e0

QD
type: SiteQuality
SIO_000300: 9.449999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.05e0

MQRankSum
type: SiteQuality
SIO_000300: -2.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4789
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.560305819940709e-5
allele num: 64090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9648
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-1

FS
type: SiteQuality
SIO_000300: 1.313e0

DP
type: SiteQuality
SIO_000300: 1.49622e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

VQSLOD
type: SiteQuality
SIO_000300: 5.16e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 42716
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2179
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variant carriers: 0

GenotypeQuality
all individuals: 3313
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.737317581653926e-4
allele num: 11512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65614
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: 9976
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.305e0

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.113e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.333e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

DP
type: SiteQuality
SIO_000300: 1.534251e6

GenotypeQuality
all individuals: 633
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2197
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1832
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42737
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5200
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3311
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 244
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523229246001523e-5
allele num: 65650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9984
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.315e0

FS
type: SiteQuality
SIO_000300: 4.134e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.73e-1

DP
type: SiteQuality
SIO_000300: 1.534984e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.198e0

GenotypeQuality
all individuals: 151
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
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variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2256
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65840
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.03e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 5.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.416e0

DP
type: SiteQuality
SIO_000300: 1.542466e6

GenotypeQuality
all individuals: 863
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 675
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variant carriers: 1

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1905
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GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 130
bin: 4.25e1
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GenotypeQuality
all individuals: 2269
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3465
bin: 9.75e1
variant carriers: 103

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42169
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 45
allele frequency: 6.83371298405467e-4
allele num: 65850
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.735809755250825e-4
allele num: 11522
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.34075723830735e-3
allele num: 898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 54
allele frequency: 8.176862507571169e-3
allele num: 6604
num of homozygotes: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.094588005850804e-5
allele num: 16408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.546106e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.68e0

QD
type: SiteQuality
SIO_000300: 1.333e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1

GenotypeQuality
all individuals: 3465
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 130
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
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GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 5.25e1
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GenotypeQuality
all individuals: 231
bin: 4.75e1
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GenotypeQuality
all individuals: 147
bin: 2.75e1
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GenotypeQuality
all individuals: 891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1905
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2269
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65850
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.321262766945218e-4
allele num: 8616
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9986
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 1.546106e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1

QD
type: SiteQuality
SIO_000300: 1.333e1

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 38

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 46

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 13

GenotypeQuality
all individuals: 200
bin: 5.25e1
variant carriers: 77

GenotypeQuality
all individuals: 183
bin: 5.75e1
variant carriers: 81

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 39

GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 117

GenotypeQuality
all individuals: 26714
bin: 9.75e1
variant carriers: 24702

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 40

GenotypeQuality
all individuals: 958
bin: 7.25e1
variant carriers: 96

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 23

GenotypeQuality
all individuals: 933
bin: 8.25e1
variant carriers: 173

GenotypeQuality
all individuals: 25368
bin: 6.25e1
variant carriers: 104

Latino
type: Population
allele count: 3126
allele frequency: 2.711658570437196e-1
allele num: 11528
num of homozygotes: 438

European (Non-Finnish)
type: Population
allele count: 20214
allele frequency: 3.058463959329419e-1
allele num: 66092
num of homozygotes: 3097

European (Finnish)
type: Population
allele count: 1927
allele frequency: 2.915279878971256e-1
allele num: 6610
num of homozygotes: 299

African
type: Population
allele count: 2429
allele frequency: 2.416434540389972e-1
allele num: 10052
num of homozygotes: 282

East Asian
type: Population
allele count: 807
allele frequency: 9.36846993266775e-2
allele num: 8614
num of homozygotes: 34

Other
type: Population
allele count: 212
allele frequency: 2.339955849889625e-1
allele num: 906
num of homozygotes: 25

South Asian
type: Population
allele count: 1561
allele frequency: 9.510174241501157e-2
allele num: 16414
num of homozygotes: 83

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.98e-2

QD
type: SiteQuality
SIO_000300: 1.511e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.555e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.83e0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

DP
type: SiteQuality
SIO_000300: 2.323334e6

GenotypeQuality
all individuals: 721
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5838
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
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GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2642
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6138
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1053
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38074
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.029017992366875e-5
allele num: 66028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
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
allele num: 16424
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQRankSum
type: SiteQuality
SIO_000300: 6.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 1.783281e6

VQSLOD
type: SiteQuality
SIO_000300: 6.39e-1

QD
type: SiteQuality
SIO_000300: 1.115e1

GenotypeQuality
all individuals: 263
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36196
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5509
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1917
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521931026085898e-5
allele num: 65706
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.025641025641026e-4
allele num: 9750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.005e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 6.802e0

DP
type: SiteQuality
SIO_000300: 1.754891e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.146e0

GenotypeQuality
all individuals: 594
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1846
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5509
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.025641025641026e-4
allele num: 9750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65706
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

QD
type: SiteQuality
SIO_000300: 1.005e1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.146e0

FS
type: SiteQuality
SIO_000300: 6.802e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 1.754891e6

GenotypeQuality
all individuals: 205
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6095
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1701
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5387
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.109481915933529e-5
allele num: 16368
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.09e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.22e-1

DP
type: SiteQuality
SIO_000300: 1.730376e6

MQ
type: SiteQuality
SIO_000300: 5.945e1

GenotypeQuality
all individuals: 695
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6096
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1076
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1953
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31207
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65560
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.110975311659741e-5
allele num: 16364
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.835e0

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

DP
type: SiteQuality
SIO_000300: 1.704267e6

QD
type: SiteQuality
SIO_000300: 1.153e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeQuality
all individuals: 2914
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28122
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4613
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1738
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.12294881214793e-5
allele num: 16332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9636
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.429e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.670287e6

QD
type: SiteQuality
SIO_000300: 1.1e1

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.45e-1

GenotypeQuality
all individuals: 6092
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27182
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3300
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2554
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
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variant carriers: 0

GenotypeQuality
all individuals: 4558
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65370
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.125199068969742e-5
allele num: 16326
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 1.664811e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.177e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.48e0

FS
type: SiteQuality
SIO_000300: 1.501e0

QD
type: SiteQuality
SIO_000300: 1.899e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.13e-1

GenotypeQuality
all individuals: 63
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4097
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2916
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23819
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4426
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2555
bin: 2.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.727526618956188e-5
allele num: 11458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.64814e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.692e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.01e-1

GenotypeQuality
all individuals: 428
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 8576
bin: 9.75e1
variant carriers: 3087

GenotypeQuality
all individuals: 297
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 22515
bin: 6.25e1
variant carriers: 9

GenotypeQuality
all individuals: 1571
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4002
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2033
bin: 7.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1501
bin: 8.25e1
variant carriers: 11

GenotypeQuality
all individuals: 982
bin: 9.25e1
variant carriers: 11

GenotypeQuality
all individuals: 152
bin: 1.25e1
variant carriers: 2

Latino
type: Population
allele count: 142
allele frequency: 1.239308779891779e-2
allele num: 11458
num of homozygotes: 1

Other
type: Population
allele count: 21
allele frequency: 2.348993288590604e-2
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 70
allele frequency: 7.297748123436197e-3
allele num: 9592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

South Asian
type: Population
allele count: 156
allele frequency: 9.567030540905188e-3
allele num: 16306
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 192
allele frequency: 2.915274825387185e-2
allele num: 6586
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 2641
allele frequency: 4.053473309390061e-2
allele num: 65154
num of homozygotes: 49

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.58e0

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

QD
type: SiteQuality
SIO_000300: 1.39e1

DP
type: SiteQuality
SIO_000300: 1.643441e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 295
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2517
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3495
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19989
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2584
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5938
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 1.046243984097091e-4
allele num: 9558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
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: 0
allele frequency: 0.0e0
allele num: 65038
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16282
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.623961e6

MQRankSum
type: SiteQuality
SIO_000300: -8.59e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.409e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.329e1

GenotypeQuality
all individuals: 872
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4136
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7991
bin: 9.75e1
variant carriers: 421

GenotypeQuality
all individuals: 1044
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 594
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variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 148
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1153
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 319
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 7.25e1
variant carriers: 4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7834
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.796163069544364e-3
allele num: 834
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.453752181500873e-4
allele num: 9168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.404098623118795e-4
allele num: 6246
num of homozygotes: 0

Latino
type: Population
allele count: 23
allele frequency: 2.152751778360165e-3
allele num: 10684
num of homozygotes: 0

South Asian
type: Population
allele count: 127
allele frequency: 8.310430571914671e-3
allele num: 15282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 268
allele frequency: 4.601174329567696e-3
allele num: 58246
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.53e0

FS
type: SiteQuality
SIO_000300: 9.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.480525e6

QD
type: SiteQuality
SIO_000300: 1.254e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.339e0

GenotypeQuality
all individuals: 585
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1949
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34509
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.236245954692556e-5
allele num: 61800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.262e1

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

DP
type: SiteQuality
SIO_000300: 1.59446e6

FS
type: SiteQuality
SIO_000300: 3.569e0

VQSLOD
type: SiteQuality
SIO_000300: 8.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1956
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7688
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 630
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.342762907522517e-5
allele num: 15766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62000
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8224
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.272e0

FS
type: SiteQuality
SIO_000300: 4.406e0

VQSLOD
type: SiteQuality
SIO_000300: 5.679999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.599591e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.618e0

MQRankSum
type: SiteQuality
SIO_000300: -3.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

QD
type: SiteQuality
SIO_000300: 1.268e1

GenotypeQuality
all individuals: 2760
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7690
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1658
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11104
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.299609424215698e-5
allele num: 15874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8300
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62876
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.267e0

MQRankSum
type: SiteQuality
SIO_000300: 9.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.617267e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-1

QD
type: SiteQuality
SIO_000300: 8.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e0

VQSLOD
type: SiteQuality
SIO_000300: -8.066e-1

GenotypeQuality
all individuals: 773
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2628
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7690
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1425
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 905
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variant carriers: 0

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

GenotypeQuality
all individuals: 184
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.58463537540012e-5
allele num: 63106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11138
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.620687e6

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.184e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-2

GenotypeQuality
all individuals: 189
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38110
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7692
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1453
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
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variant carriers: 0

GenotypeQuality
all individuals: 150
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variant carriers: 0

GenotypeQuality
all individuals: 5292
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540215014015957e-5
allele num: 64926
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.841e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 9.9e-1

QD
type: SiteQuality
SIO_000300: 2.039e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.621e0

DP
type: SiteQuality
SIO_000300: 1.656926e6

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
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variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 159
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variant carriers: 0

GenotypeQuality
all individuals: 312
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variant carriers: 0

GenotypeQuality
all individuals: 189
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GenotypeQuality
all individuals: 5333
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7692
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65160
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.179801793298726e-4
allele num: 8476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16184
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.836e1

VQSLOD
type: SiteQuality
SIO_000300: -2.081e0

DP
type: SiteQuality
SIO_000300: 1.660695e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

QD
type: SiteQuality
SIO_000300: 1.135e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.027e0

GenotypeQuality
all individuals: 38365
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1759
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
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GenotypeQuality
all individuals: 175
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5344
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2072
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7691
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.788566953797964e-5
allele num: 10216
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65344
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.982e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.77e0

QD
type: SiteQuality
SIO_000300: 1.185e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.76e-1

DP
type: SiteQuality
SIO_000300: 1.664899e6

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

FS
type: SiteQuality
SIO_000300: 2.317e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

GenotypeQuality
all individuals: 5361
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
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variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2071
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variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528537800739812e-5
allele num: 65422
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.666554e6

QD
type: SiteQuality
SIO_000300: 1.794e1

GenotypeQuality
all individuals: 648
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 267
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524762137106611e-5
allele num: 65584
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: 11420
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16248
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.159e1

DP
type: SiteQuality
SIO_000300: 1.670031e6

VQSLOD
type: SiteQuality
SIO_000300: 2.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.508e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5392
bin: 6.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.570383912248629e-5
allele num: 65640
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.078e0

DP
type: SiteQuality
SIO_000300: 1.671488e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e-1

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

QD
type: SiteQuality
SIO_000300: 1.14e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

African
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allele frequency: 9.731413001167769e-5
allele num: 10276
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65810
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 8.093e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.216e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.6749e6

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.274e1

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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 1
allele frequency: 9.695559433779329e-5
allele num: 10314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.169043722235212e-4
allele num: 8554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66214
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

DP
type: SiteQuality
SIO_000300: 1.695161e6

FS
type: SiteQuality
SIO_000300: 5.689e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.593e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.53e-1

MQ
type: SiteQuality
SIO_000300: 6.008e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 1
allele frequency: 1.168497312456181e-4
allele num: 8558
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.940617116242965e-4
allele num: 10306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66262
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.41e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

FS
type: SiteQuality
SIO_000300: 1.155e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.695325e6

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: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66290
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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QD
type: SiteQuality
SIO_000300: 1.587e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.6966e6

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.3e0

VQSLOD
type: SiteQuality
SIO_000300: -5.006e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.48e-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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.087168249330411e-5
allele num: 16428
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66320
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e-1

BaseQRankSum
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SIO_000300: -4.06e0

InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.698802e6

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 9.706853038245001e-5
allele num: 10302
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 902
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: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507159005275056e-5
allele num: 66350
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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BaseQRankSum
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MQ
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MQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.41e-2

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 1

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

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

African
type: Population
allele count: 1
allele frequency: 9.706853038245001e-5
allele num: 10302
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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Latino
type: Population
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allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

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

QD
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

GenotypeQuality
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variant carriers: 1

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

East Asian
type: Population
allele count: 1
allele frequency: 1.168497312456181e-4
allele num: 8558
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66390
num of homozygotes: 0

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 1465
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39566
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.700191404210893e-5
allele num: 11494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66314
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -5.152e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.364e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.72e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.700052e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 864
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5421
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variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7739
bin: 9.75e1
variant carriers: 55

GenotypeQuality
all individuals: 642
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39241
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.980982567353407e-4
allele num: 10096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.519756838905775e-4
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 51
allele frequency: 7.707420281094151e-4
allele num: 66170
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.722958827634333e-5
allele num: 11464
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

FS
type: SiteQuality
SIO_000300: 1.796e0

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

QD
type: SiteQuality
SIO_000300: 1.156e1

DP
type: SiteQuality
SIO_000300: 1.697783e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

GenotypeQuality
all individuals: 39147
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 124
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variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2042
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 34
allele frequency: 5.139678316604184e-4
allele num: 66152
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.590000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.089e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

DP
type: SiteQuality
SIO_000300: 1.697177e6

VQSLOD
type: SiteQuality
SIO_000300: 2.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.07e-1

MQ
type: SiteQuality
SIO_000300: 6.019e1

GenotypeQuality
all individuals: 1124
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5385
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variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 7692
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variant carriers: 1

GenotypeQuality
all individuals: 643
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
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variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38809
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variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 9.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.996001599360256e-5
allele num: 10004
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66022
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.43e-1

FS
type: SiteQuality
SIO_000300: 6.629e0

VQSLOD
type: SiteQuality
SIO_000300: -1.174e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.854e1

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 1.689845e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

GenotypeQuality
all individuals: 1695
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5177
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
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variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35834
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7767
bin: 9.75e1
variant carriers: 81

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

Latino
type: Population
allele count: 79
allele frequency: 6.923751095530237e-3
allele num: 11410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.048780487804878e-5
allele num: 65600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.84e-1

QD
type: SiteQuality
SIO_000300: 1.5e1

FS
type: SiteQuality
SIO_000300: 1.298e0

DP
type: SiteQuality
SIO_000300: 1.66228e6

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.1e0

GenotypeQuality
all individuals: 1933
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35770
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variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5177
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525273786644703e-5
allele num: 65562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 9.98e0

DP
type: SiteQuality
SIO_000300: 1.657924e6

VQSLOD
type: SiteQuality
SIO_000300: -2.836e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.323e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-1

GenotypeQuality
all individuals: 341
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
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variant carriers: 0

GenotypeQuality
all individuals: 909
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variant carriers: 0

GenotypeQuality
all individuals: 1419
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variant carriers: 0

GenotypeQuality
all individuals: 1970
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23640
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4650
bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539266693347289e-5
allele num: 64966
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16340
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.94e1

QD
type: SiteQuality
SIO_000300: 1.24e1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.582654e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

GenotypeQuality
all individuals: 4546
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1934
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variant carriers: 0

GenotypeQuality
all individuals: 541
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variant carriers: 0

GenotypeQuality
all individuals: 4467
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16482
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2473
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variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1419
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549426712116517e-5
allele num: 64540
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.954e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 3.358e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.093e0

VQSLOD
type: SiteQuality
SIO_000300: -3.971e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

DP
type: SiteQuality
SIO_000300: 1.584743e6

GenotypeQuality
all individuals: 3154
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8976
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 2254
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variant carriers: 0

GenotypeQuality
all individuals: 4388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10906
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1487
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variant carriers: 0

GenotypeQuality
all individuals: 25431
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 4
allele frequency: 3.460806367883717e-4
allele num: 11558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.226622e6

MQ
type: SiteQuality
SIO_000300: 5.437e1

QD
type: SiteQuality
SIO_000300: 1.76e1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 2.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.919e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.05e-1

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2253
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 8975
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1486
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3155
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10899
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

Other
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QD
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MQ
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MQRankSum
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VQSLOD
type: SiteQuality
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FS
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SIO_000300: 9.69e-1

InbreedingCoeff
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SIO_000300: 1.0e-3

BaseQRankSum
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SIO_000300: -2.458e0

ClippingRankSum
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ReadPosRankSum
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DP
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GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11554
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.69e-1

BaseQRankSum
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SIO_000300: -2.458e0

ReadPosRankSum
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MQRankSum
type: SiteQuality
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QD
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DP
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele num: 10400
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.000570108320581e-5
allele num: 66654
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

FS
type: SiteQuality
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DP
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ClippingRankSum
type: SiteQuality
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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SIO_000300: 5.92e1

BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 1.156604210039325e-4
allele num: 8646
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11572
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Other
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South Asian
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allele count: 0
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African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.998231043684226e-5
allele num: 66706
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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SIO_000300: -9.71e-1

ReadPosRankSum
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.231151e6

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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East Asian
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allele count: 2
allele frequency: 2.312673450508788e-4
allele num: 8648
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66712
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
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MQ
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Non-Finnish)
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allele num: 66724
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Latino
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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FS
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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DP
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MQRankSum
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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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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 2.997152704930316e-5
allele num: 66730
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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num of homozygotes: 0

East Asian
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African
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Other
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South Asian
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ReadPosRankSum
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MQRankSum
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QD
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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DP
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MQ
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BaseQRankSum
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FS
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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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GenotypeQuality
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European (Finnish)
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Latino
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East Asian
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South Asian
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African
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Other
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European (Non-Finnish)
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allele frequency: 1.498621268433042e-5
allele num: 66728
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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African
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Other
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Latino
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allele frequency: 8.637070305752289e-5
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ClippingRankSum
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FS
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InbreedingCoeff
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QD
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ReadPosRankSum
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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GenotypeQuality
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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: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26201
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3316
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
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: 6608
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.231744e6

VQSLOD
type: SiteQuality
SIO_000300: 6.830000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.5e0

FS
type: SiteQuality
SIO_000300: 9.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.129e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-1

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9016
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3142
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.217e0

QD
type: SiteQuality
SIO_000300: 1.266e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.232037e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3316
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3142
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26202
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1488
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.217e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

DP
type: SiteQuality
SIO_000300: 2.232037e6

QD
type: SiteQuality
SIO_000300: 1.266e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3316
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3142
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.787e0

FS
type: SiteQuality
SIO_000300: 1.927e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.335e1

DP
type: SiteQuality
SIO_000300: 2.231723e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10890
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1488
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
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: 11578
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: 6612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.328e0

QD
type: SiteQuality
SIO_000300: 9.7e-1

FS
type: SiteQuality
SIO_000300: 9.666e0

DP
type: SiteQuality
SIO_000300: 2.231707e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.673e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.81e-1

MQ
type: SiteQuality
SIO_000300: 5.364e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.37e-2