17-18150723-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18150723
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18150723
    reference: chr 17
allele count: 193
allele frequency: 1.705067495936109e-3
allele num: 113192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2439-52C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2323-52C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1718C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.508-52C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2455-52C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1420C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000459958
  gene symbol: FLII
  hgvsc: ENST00000459958.2:n.28C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2230-52C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2488-52C>G
  variant of: http://identifiers.org/hgnc/3750
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 37178
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 3.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33336
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2133
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 2.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

17-18150923-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18150923
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18150923
    reference: chr 17
allele count: 4
allele frequency: 1.216397031991242e-4
allele num: 32884
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2454+48G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1620G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.507+48G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2322+48G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2438+48G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2229+48G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1518G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2487+48G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14008
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13290
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 28908
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5369
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5728
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8301
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

17-18150931-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18150931
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18150931
    reference: chr 17
allele count: 1
allele frequency: 2.912564804566902e-5
allele num: 34334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2438+40C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.507+40C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1628C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2322+40C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2229+40C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1510C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2454+40C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2487+40C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29807
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3969
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10228
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

17-18150931-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18150931
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18150931
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 34334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1628C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1510C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2454+40C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2322+40C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.507+40C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2487+40C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2229+40C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2438+40C>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29807
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4928
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24840
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3653
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

17-18150940-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18150940
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18150940
    reference: chr 17
allele count: 1
allele frequency: 2.710320901994796e-5
allele num: 36896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1637A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2454+31A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2322+31A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2229+31A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.507+31A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1501A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2438+31A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2487+31A>G
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13055
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31889
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1861
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2086
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3357
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4946
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

17-18150940-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18150940
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18150939
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 36896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2229+30delC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2322+30delC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2454+30delC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.507+30delC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1638delC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1500delC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2438+30delC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2487+30delC
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13055
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31889
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4946
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2086
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8232
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: TG
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

17-18150966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18150966
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18150966
    reference: chr 17
allele count: 3
allele frequency: 5.010522096402445e-5
allele num: 59874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1475G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2322+5G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2454+5G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2438+5G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2229+5G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2487+5G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1663G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.507+5G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18538
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25974
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
hgvs: c.2487+5G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

17-18150970-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18150970
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18150970
    reference: chr 17
allele count: 1
allele frequency: 1.510802235987309e-5
allele num: 66190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1667G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1471G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.507+1G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2322+1G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2487+1G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2229+1G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2438+1G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2454+1G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23813
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3229
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
hgvs: c.2487+1G>A
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-18150988-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18150988
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18150988
    reference: chr 17
allele count: 11
allele frequency: 1.24634594031136e-4
allele num: 88258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2437G>C
  hgvsp: ENSP00000463534.1:p.Glu813Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2305G>C
  hgvsp: ENSP00000438536.2:p.Glu769Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2470G>C
  hgvsp: ENSP00000324573.4:p.Glu824Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1453G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2421G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2212G>C
  hgvsp: ENSP00000368763.4:p.Glu738Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1685G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.490G>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32225
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13669
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2267
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu824Gln
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

17-18150996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18150996
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18150996
    reference: chr 17
allele count: 2
allele frequency: 2.087029114056141e-5
allele num: 95830
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2462G>A
  hgvsp: ENSP00000324573.4:p.Arg821His
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2204G>A
  hgvsp: ENSP00000368763.4:p.Arg735His
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1693G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2429G>A
  hgvsp: ENSP00000463534.1:p.Arg810His
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2297G>A
  hgvsp: ENSP00000438536.2:p.Arg766His
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1445G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2413G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.482G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2843
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2037
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1242
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg821His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

17-18151009-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151009
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151009
    reference: chr 17
allele count: 11
allele frequency: 1.083082255174179e-4
allele num: 101562
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2449G>A
  hgvsp: ENSP00000324573.4:p.Ala817Thr
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.469G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2191G>A
  hgvsp: ENSP00000368763.4:p.Ala731Thr
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2416G>A
  hgvsp: ENSP00000463534.1:p.Ala806Thr
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2400G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2284G>A
  hgvsp: ENSP00000438536.2:p.Ala762Thr
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1706G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1432G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7398
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32949
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9677
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8301
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2927
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1906
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 9.75e1
  variant carriers: 10
hgvs: p.Ala817Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

17-18151021-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151021
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151021
    reference: chr 17
allele count: 2
allele frequency: 1.916406354803473e-5
allele num: 104362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2272C>A
  hgvsp: ENST00000545457.2:c.2272C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2437C>A
  hgvsp: ENST00000327031.4:c.2437C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1718C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.457C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2179C>A
  hgvsp: ENST00000379450.4:c.2179C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2388C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1420C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2404C>A
  hgvsp: ENST00000579294.1:c.2404C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10623
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1660
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3467
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg813Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

17-18151022-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151022
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151022
    reference: chr 17
allele count: 12
allele frequency: 1.142617737236008e-4
allele num: 105022
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2436C>T
  hgvsp: ENST00000327031.4:c.2436C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1419C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2178C>T
  hgvsp: ENST00000379450.4:c.2178C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1719C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2403C>T
  hgvsp: ENST00000579294.1:c.2403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.456C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2271C>T
  hgvsp: ENST00000545457.2:c.2271C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2387C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10693
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33196
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7086
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1438
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His812His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-18151023-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151023
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151023
    reference: chr 17
allele count: 5
allele frequency: 4.880715317636953e-5
allele num: 102444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2177A>C
  hgvsp: ENSP00000368763.4:p.His726Pro
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2435A>C
  hgvsp: ENSP00000324573.4:p.His812Pro
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2270A>C
  hgvsp: ENSP00000438536.2:p.His757Pro
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1720A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2402A>C
  hgvsp: ENSP00000463534.1:p.His801Pro
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1418A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.455A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2386A>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32093
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10193
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1716
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 1.75e1
  variant carriers: 1
hgvs: p.His812Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-18151033-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151033
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151033
    reference: chr 17
allele count: 9
allele frequency: 8.370068634562804e-5
allele num: 107526
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2425G>C
  hgvsp: ENSP00000324573.4:p.Gly809Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1408G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2376G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2167G>C
  hgvsp: ENSP00000368763.4:p.Gly723Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2392G>C
  hgvsp: ENSP00000463534.1:p.Gly798Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.445G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2260G>C
  hgvsp: ENSP00000438536.2:p.Gly754Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1730G>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12094
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33811
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1268
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5891
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4053
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly809Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

17-18151034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151034
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151034
    reference: chr 17
allele count: 8
allele frequency: 7.433424392782145e-5
allele num: 107622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2166C>T
  hgvsp: ENST00000379450.4:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2424C>T
  hgvsp: ENST00000327031.4:c.2424C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1407C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2375C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.444C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2259C>T
  hgvsp: ENST00000545457.2:c.2259C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2391C>T
  hgvsp: ENST00000579294.1:c.2391C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1731C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12240
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys808Cys
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

17-18151044-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151044
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151044
    reference: chr 17
allele count: 12
allele frequency: 1.094870531559643e-4
allele num: 109602
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2249A>G
  hgvsp: ENSP00000438536.2:p.Gln750Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1741A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2156A>G
  hgvsp: ENSP00000368763.4:p.Gln719Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2381A>G
  hgvsp: ENSP00000463534.1:p.Gln794Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2365A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.434A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1397A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2414A>G
  hgvsp: ENSP00000324573.4:p.Gln805Arg
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13245
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35080
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5026
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln805Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

17-18151047-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151047
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151047
    reference: chr 17
allele count: 1
allele frequency: 9.088760838347299e-6
allele num: 110026
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.431G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2246G>A
  hgvsp: ENSP00000438536.2:p.Gly749Asp
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2362G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1394G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1744G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2411G>A
  hgvsp: ENSP00000324573.4:p.Gly804Asp
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2153G>A
  hgvsp: ENSP00000368763.4:p.Gly718Asp
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2378G>A
  hgvsp: ENSP00000463534.1:p.Gly793Asp
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13518
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4962
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly804Asp
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/17-18151048-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151048
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151048
    reference: chr 17
allele count: 1
allele frequency: 9.076881183625307e-6
allele num: 110170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1393G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2245G>T
  hgvsp: ENSP00000438536.2:p.Gly749Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2377G>T
  hgvsp: ENSP00000463534.1:p.Gly793Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2410G>T
  hgvsp: ENSP00000324573.4:p.Gly804Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1745G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2361G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2152G>T
  hgvsp: ENSP00000368763.4:p.Gly718Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.430G>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44070
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly804Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

17-18151051-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151051
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151051
    reference: chr 17
allele count: 1
allele frequency: 9.050428990334141e-6
allele num: 110492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1390C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1748C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.427C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2358C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2374C>T
  hgvsp: ENST00000579294.1:c.2374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2242C>T
  hgvsp: ENST00000545457.2:c.2242C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2149C>T
  hgvsp: ENST00000379450.4:c.2149C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2407C>T
  hgvsp: ENST00000327031.4:c.2407C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu803Leu
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

17-18151051-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151051
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151051
    reference: chr 17
allele count: 1
allele frequency: 9.050428990334141e-6
allele num: 110492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1390C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2149C>A
  hgvsp: ENSP00000368763.4:p.Leu717Met
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.427C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2374C>A
  hgvsp: ENSP00000463534.1:p.Leu792Met
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1748C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2358C>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2407C>A
  hgvsp: ENSP00000324573.4:p.Leu803Met
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2242C>A
  hgvsp: ENSP00000438536.2:p.Leu748Met
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13801
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4701
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 909
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu803Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

17-18151054-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151054
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151054
    reference: chr 17
allele count: 7
allele frequency: 6.314384167132728e-5
allele num: 110858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2239A>C
  hgvsp: ENSP00000438536.2:p.Lys747Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2404A>C
  hgvsp: ENSP00000324573.4:p.Lys802Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2146A>C
  hgvsp: ENSP00000368763.4:p.Lys716Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2355A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1387A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2371A>C
  hgvsp: ENSP00000463534.1:p.Lys791Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.424A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1751A>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14016
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35034
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4401
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys802Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

17-18151061-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151061
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151061
    reference: chr 17
allele count: 4
allele frequency: 3.582110937975749e-5
allele num: 111666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2139C>T
  hgvsp: ENST00000379450.4:c.2139C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.417C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2397C>T
  hgvsp: ENST00000327031.4:c.2397C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2348C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1380C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2364C>T
  hgvsp: ENST00000579294.1:c.2364C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1758C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2232C>T
  hgvsp: ENST00000545457.2:c.2232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14483
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44172
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala799Ala
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

17-18151069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151069
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151069
    reference: chr 17
allele count: 1
allele frequency: 8.872957001650369e-6
allele num: 112702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1372C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2389C>T
  hgvsp: ENSP00000324573.4:p.Arg797Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2340C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.409C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2356C>T
  hgvsp: ENSP00000463534.1:p.Arg786Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1766C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2224C>T
  hgvsp: ENSP00000438536.2:p.Arg742Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2131C>T
  hgvsp: ENSP00000368763.4:p.Arg711Cys
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35028
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg797Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

17-18151078-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151078
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151078
    reference: chr 17
allele count: 6
allele frequency: 5.274910766092873e-5
allele num: 113746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2347C>T
  hgvsp: ENSP00000463534.1:p.Arg783Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1775C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2215C>T
  hgvsp: ENSP00000438536.2:p.Arg739Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2331C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2380C>T
  hgvsp: ENSP00000324573.4:p.Arg794Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2122C>T
  hgvsp: ENSP00000368763.4:p.Arg708Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.400C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1363C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2669
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35211
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4634
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45402
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg794Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

17-18151087-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151087
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151087
    reference: chr 17
allele count: 3
allele frequency: 2.60556896941062e-5
allele num: 115138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1354A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1784A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2206A>G
  hgvsp: ENSP00000438536.2:p.Lys736Glu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2338A>G
  hgvsp: ENSP00000463534.1:p.Lys780Glu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2113A>G
  hgvsp: ENSP00000368763.4:p.Lys705Glu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2371A>G
  hgvsp: ENSP00000324573.4:p.Lys791Glu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.391A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2322A>G
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46821
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys791Glu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

17-18151090-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151090
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151090
    reference: chr 17
allele count: 1
allele frequency: 8.657259111765215e-6
allele num: 115510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.388C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1351C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2203C>T
  hgvsp: ENSP00000438536.2:p.Arg735Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2335C>T
  hgvsp: ENSP00000463534.1:p.Arg779Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1787C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2110C>T
  hgvsp: ENSP00000368763.4:p.Arg704Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2368C>T
  hgvsp: ENSP00000324573.4:p.Arg790Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2319C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47058
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg790Cys
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

17-18151094-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151094
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151094
    reference: chr 17
allele count: 1
allele frequency: 8.599043786330961e-6
allele num: 116292
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2364C>T
  hgvsp: ENST00000327031.4:c.2364C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.384C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2331C>T
  hgvsp: ENST00000579294.1:c.2331C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1791C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2199C>T
  hgvsp: ENST00000545457.2:c.2199C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2315C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1347C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2106C>T
  hgvsp: ENST00000379450.4:c.2106C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2663
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47956
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4908
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu788Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

17-18151099-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151099
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151099
    reference: chr 17
allele count: 12
allele frequency: 1.024572667816465e-4
allele num: 117122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2101T>A
  hgvsp: ENSP00000368763.4:p.Trp701Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1342T>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2194T>A
  hgvsp: ENSP00000438536.2:p.Trp732Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2359T>A
  hgvsp: ENSP00000324573.4:p.Trp787Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2326T>A
  hgvsp: ENSP00000463534.1:p.Trp776Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.379T>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1796T>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2310T>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16920
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Trp787Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

17-18151108-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151108
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151108
    reference: chr 17
allele count: 26
allele frequency: 2.2069059179031e-4
allele num: 117812
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2185G>A
  hgvsp: ENSP00000438536.2:p.Val729Met
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2317G>A
  hgvsp: ENSP00000463534.1:p.Val773Met
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.370G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2301G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2092G>A
  hgvsp: ENSP00000368763.4:p.Val698Met
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1805G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2350G>A
  hgvsp: ENSP00000324573.4:p.Val784Met
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1333G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17166
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36826
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1943
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 9.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val784Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-18151109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151109
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151109
    reference: chr 17
allele count: 1
allele frequency: 8.481332586976066e-6
allele num: 117906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2316C>T
  hgvsp: ENST00000579294.1:c.2316C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2300C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2349C>T
  hgvsp: ENST00000327031.4:c.2349C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.369C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2184C>T
  hgvsp: ENST00000545457.2:c.2184C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2091C>T
  hgvsp: ENST00000379450.4:c.2091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1332C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1806C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36828
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5074
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49007
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp783Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

17-18151115-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151115
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151115
    reference: chr 17
allele count: 1
allele frequency: 8.439103429651633e-6
allele num: 118496
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.363G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2343G>C
  hgvsp: ENSP00000324573.4:p.Trp781Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2085G>C
  hgvsp: ENSP00000368763.4:p.Trp695Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2310G>C
  hgvsp: ENSP00000463534.1:p.Trp770Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1326G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2294G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2178G>C
  hgvsp: ENSP00000438536.2:p.Trp726Cys
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1812G>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49335
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5135
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Trp781Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-18151116-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151116
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151116
    reference: chr 17
allele count: 1
allele frequency: 8.434405627435435e-6
allele num: 118562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1813G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2342G>T
  hgvsp: ENSP00000324573.4:p.Trp781Leu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2293G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2177G>T
  hgvsp: ENSP00000438536.2:p.Trp726Leu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2309G>T
  hgvsp: ENSP00000463534.1:p.Trp770Leu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2084G>T
  hgvsp: ENSP00000368763.4:p.Trp695Leu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1325G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.362G>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1572
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5132
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Trp781Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

17-18151117-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151117
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151117
    reference: chr 17
allele count: 1
allele frequency: 8.426445556735258e-6
allele num: 118674
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1814T>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2083T>A
  hgvsp: ENSP00000368763.4:p.Trp695Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2292T>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.361T>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2176T>A
  hgvsp: ENSP00000438536.2:p.Trp726Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2308T>A
  hgvsp: ENSP00000463534.1:p.Trp770Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2341T>A
  hgvsp: ENSP00000324573.4:p.Trp781Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1324T>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Trp781Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

17-18151129-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151129
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151129
    reference: chr 17
allele count: 29
allele frequency: 2.431009623444992e-4
allele num: 119292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2071A>C
  hgvsp: ENSP00000368763.4:p.Ile691Leu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1826A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1312A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2329A>C
  hgvsp: ENSP00000324573.4:p.Ile777Leu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2296A>C
  hgvsp: ENSP00000463534.1:p.Ile766Leu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.349A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2164A>C
  hgvsp: ENSP00000438536.2:p.Ile722Leu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2280A>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36983
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17939
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile777Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

17-18151136-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151136
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151136
    reference: chr 17
allele count: 1
allele frequency: 8.368340892734607e-6
allele num: 119498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2064C>T
  hgvsp: ENST00000379450.4:c.2064C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2322C>T
  hgvsp: ENST00000327031.4:c.2322C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.342C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2273C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1305C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2289C>T
  hgvsp: ENST00000579294.1:c.2289C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1833C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2157C>T
  hgvsp: ENST00000545457.2:c.2157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18213
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys774Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-18151142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151142
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151142
    reference: chr 17
allele count: 6
allele frequency: 5.010438413361169e-5
allele num: 119750
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2316G>A
  hgvsp: ENST00000327031.4:c.2316G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.336G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2283G>A
  hgvsp: ENST00000579294.1:c.2283G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2267G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1839G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2058G>A
  hgvsp: ENST00000379450.4:c.2058G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2151G>A
  hgvsp: ENST00000545457.2:c.2151G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1299G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36714
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr772Thr
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

17-18151145-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151145
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151145
    reference: chr 17
allele count: 3
allele frequency: 2.501626056937009e-5
allele num: 119922
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1296C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2313C>G
  hgvsp: ENSP00000324573.4:p.Asp771Glu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1842C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2280C>G
  hgvsp: ENSP00000463534.1:p.Asp760Glu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2264C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2055C>G
  hgvsp: ENSP00000368763.4:p.Asp685Glu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2148C>G
  hgvsp: ENSP00000438536.2:p.Asp716Glu
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.333C>G
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp771Glu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

17-18151149-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151149
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151149
    reference: chr 17
allele count: 18
allele frequency: 1.49947518368571e-4
allele num: 120042
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1846T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2309T>C
  hgvsp: ENSP00000324573.4:p.Leu770Pro
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2276T>C
  hgvsp: ENSP00000463534.1:p.Leu759Pro
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.329T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2051T>C
  hgvsp: ENSP00000368763.4:p.Leu684Pro
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1292T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2144T>C
  hgvsp: ENSP00000438536.2:p.Leu715Pro
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2260T>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu770Pro
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP

17-18151149-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151149
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151149
    reference: chr 17
allele count: 1
allele frequency: 8.330417687142833e-6
allele num: 120042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2276T>A
  hgvsp: ENSP00000463534.1:p.Leu759Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2309T>A
  hgvsp: ENSP00000324573.4:p.Leu770Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2051T>A
  hgvsp: ENSP00000368763.4:p.Leu684Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.329T>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2144T>A
  hgvsp: ENSP00000438536.2:p.Leu715Gln
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1846T>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2260T>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1292T>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36782
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50724
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu770Gln
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

17-18151150-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151150
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151150
    reference: chr 17
allele count: 3
allele frequency: 2.499000399840064e-5
allele num: 120048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.328C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2275C>T
  hgvsp: ENST00000579294.1:c.2275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1847C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2050C>T
  hgvsp: ENST00000379450.4:c.2050C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2308C>T
  hgvsp: ENST00000327031.4:c.2308C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2143C>T
  hgvsp: ENST00000545457.2:c.2143C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1291C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2259C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50349
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu770Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

17-18151151-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151151
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151151
    reference: chr 17
allele count: 1
allele frequency: 8.326949338840222e-6
allele num: 120092
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2142G>C
  hgvsp: ENST00000545457.2:c.2142G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2307G>C
  hgvsp: ENST00000327031.4:c.2307G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.327G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2258G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1290G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2049G>C
  hgvsp: ENST00000379450.4:c.2049G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2274G>C
  hgvsp: ENST00000579294.1:c.2274G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1848G>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu769Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

17-18151151-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151151
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151151
    reference: chr 17
allele count: 1
allele frequency: 8.326949338840222e-6
allele num: 120092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2049G>A
  hgvsp: ENST00000379450.4:c.2049G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2142G>A
  hgvsp: ENST00000545457.2:c.2142G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1290G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.327G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2274G>A
  hgvsp: ENST00000579294.1:c.2274G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2307G>A
  hgvsp: ENST00000327031.4:c.2307G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1848G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2258G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5291
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu769Leu
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-18151154-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151154
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151154
    reference: chr 17
allele count: 1
allele frequency: 8.318775476249896e-6
allele num: 120210
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1851T>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1287T>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2304T>G
  hgvsp: ENSP00000324573.4:p.Ser768Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.324T>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2139T>G
  hgvsp: ENSP00000438536.2:p.Ser713Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2046T>G
  hgvsp: ENSP00000368763.4:p.Ser682Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2271T>G
  hgvsp: ENSP00000463534.1:p.Ser757Arg
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2255T>G
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36774
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser768Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

17-18151155-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151155
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151155
    reference: chr 17
allele count: 1
allele frequency: 8.316976612661764e-6
allele num: 120236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2254G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2303G>C
  hgvsp: ENSP00000324573.4:p.Ser768Thr
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1286G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.323G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2138G>C
  hgvsp: ENSP00000438536.2:p.Ser713Thr
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1852G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2045G>C
  hgvsp: ENSP00000368763.4:p.Ser682Thr
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2270G>C
  hgvsp: ENSP00000463534.1:p.Ser757Thr
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18984
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5308
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser768Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

17-18151156-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151156
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151156
    reference: chr 17
allele count: 1
allele frequency: 8.314487162431821e-6
allele num: 120272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2253A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2269A>G
  hgvsp: ENSP00000463534.1:p.Ser757Gly
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.322A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1853A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2302A>G
  hgvsp: ENSP00000324573.4:p.Ser768Gly
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2044A>G
  hgvsp: ENSP00000368763.4:p.Ser682Gly
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1285A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2137A>G
  hgvsp: ENSP00000438536.2:p.Ser713Gly
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51012
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser768Gly
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-18151162-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151162
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151162
    reference: chr 17
allele count: 1
allele frequency: 8.306337735692333e-6
allele num: 120390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038C>T
  hgvsp: ENST00000379450.4:c.2038C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131C>T
  hgvsp: ENST00000545457.2:c.2131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296C>T
  hgvsp: ENST00000327031.4:c.2296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263C>T
  hgvsp: ENST00000579294.1:c.2263C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1859C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1279C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: c.2296C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/17-18151163-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151163
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151163
    reference: chr 17
allele count: 1
allele frequency: 8.305233958440609e-6
allele num: 120406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-1G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-1G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-1G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1860G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-1G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-1G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1278G>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-1G>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36632
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50968
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
hgvs: c.2296-1G>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

17-18151164-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151164
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151164
    reference: chr 17
allele count: 2
allele frequency: 1.660715768496222e-5
allele num: 120430
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-2A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-2A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-2A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-2A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1861A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-2A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-2A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1277A>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51053
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
hgvs: c.2296-2A>C
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: T
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

17-18151167-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151167
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151167
    reference: chr 17
allele count: 5
allele frequency: 4.149790850541133e-5
allele num: 120488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-5C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-5C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1274C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-5C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-5C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1864C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-5C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-5C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.75e1
  variant carriers: 0
hgvs: c.2296-5C>T
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

17-18151172-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151172
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151172
    reference: chr 17
allele count: 69
allele frequency: 5.721013531440701e-4
allele num: 120608
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-10C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-10C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-10C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1869C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1269C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-10C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-10C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-10C>G
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 19455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36498
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5362
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51391
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 9.75e1
  variant carriers: 67
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 2
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

17-18151172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151172
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151172
    reference: chr 17
allele count: 1
allele frequency: 8.29132395860971e-6
allele num: 120608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-10C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1269C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1869C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-10C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-10C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-10C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-10C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-10C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

17-18151178-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151178
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151178
    reference: chr 17
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-16G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-16G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-16G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1263G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-16G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1875G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-16G>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-16G>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51681
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5435
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

17-18151178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151178
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151178
    reference: chr 17
allele count: 2
allele frequency: 1.656232402530723e-5
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1875G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-16G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-16G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-16G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-16G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1263G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-16G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-16G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5435
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51681
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

17-18151183-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151183
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151183
    reference: chr 17
allele count: 1
allele frequency: 8.274994621253496e-6
allele num: 120846
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1880C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-21C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-21C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-21C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-21C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-21C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1258C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-21C>G
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51806
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-18151197-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151197
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151198
    reference: chr 17
allele count: 1
allele frequency: 8.264326209484141e-6
allele num: 121002
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-36dupT
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1895dupT
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-36dupT
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-36dupT
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1243dupT
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-36dupT
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-36dupT
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-36dupT
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5464
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

17-18151199-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151199
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151199
    reference: chr 17
allele count: 4
allele frequency: 3.305184181388508e-5
allele num: 121022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-37T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-37T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-37T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1896T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1242T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-37T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-37T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-37T>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 52056
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5471
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD

17-18151200-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151200
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151200
    reference: chr 17
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-38G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1241G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-38G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-38G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-38G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1897G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-38G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-38G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

17-18151200-CGG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151200
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151198
    reference: chr 17
allele count: 3
allele frequency: 2.478888136041381e-5
allele num: 121022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1239_1931+1240delCC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-40_316-39delCC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-40_2038-39delCC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1899_218-1898delCC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-40_2296-39delCC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-40_*2247-39delCC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-40_2263-39delCC
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-40_2131-39delCC
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5464
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: CGG
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

17-18151202-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151202
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151202
    reference: chr 17
allele count: 1
allele frequency: 8.260912665631299e-6
allele num: 121052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.316-40C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2038-40C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2263-40C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2247-40C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1239C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2131-40C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1899C>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2296-40C>G
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

17-18151206-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151206
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151206
    reference: chr 17
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2130+37C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1235C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1903C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2295+37C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.315+37C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2037+37C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2262+37C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2246+37C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5488
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

17-18151225-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151225
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151225
    reference: chr 17
allele count: 2
allele frequency: 1.649974425396406e-5
allele num: 121214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2246+18A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2262+18A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2295+18A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1216A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.315+18A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2037+18A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2130+18A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1922A>G
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

17-18151230-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151230
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151230
    reference: chr 17
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2130+13G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1927G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.315+13G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1211G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2037+13G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2295+13G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2262+13G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2246+13G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52347
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

17-18151232-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151232
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151232
    reference: chr 17
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.315+11C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2295+11C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2037+11C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2246+11C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1929C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1209C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2130+11C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2262+11C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

17-18151234-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151234
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151234
    reference: chr 17
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2037+9T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1207T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2130+9T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2246+9T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1931T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2295+9T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.315+9T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2262+9T>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5513
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

17-18151237-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151237
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151237
    reference: chr 17
allele count: 3
allele frequency: 2.473614775725594e-5
allele num: 121280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.315+6A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1204A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2262+6A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2130+6A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2295+6A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2037+6A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1934A>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2246+6A>C
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
hgvs: c.2295+6A>C
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

17-18151240-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151240
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151240
    reference: chr 17
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1201A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2295+3A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2262+3A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2037+3A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.315+3A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1937A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2130+3A>G
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2246+3A>G
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36548
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
hgvs: c.2295+3A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

17-18151245-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151245
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151245
    reference: chr 17
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2244C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2260C>T
  hgvsp: ENST00000579294.1:c.2260C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2035C>T
  hgvsp: ENST00000379450.4:c.2035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1942C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2128C>T
  hgvsp: ENST00000545457.2:c.2128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.313C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1196C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2293C>T
  hgvsp: ENST00000327031.4:c.2293C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
hgvs: c.2293C>T
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

17-18151248-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151248
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151248
    reference: chr 17
allele count: 2
allele frequency: 1.64866870002473e-5
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2125C>T
  hgvsp: ENSP00000438536.2:p.Arg709Trp
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2257C>T
  hgvsp: ENSP00000463534.1:p.Arg753Trp
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2032C>T
  hgvsp: ENSP00000368763.4:p.Arg678Trp
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.310C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1945C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1193C>T
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2290C>T
  hgvsp: ENSP00000324573.4:p.Arg764Trp
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2241C>T
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg764Trp
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-18151259-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151259
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151259
    reference: chr 17
allele count: 3
allele frequency: 2.472595400972554e-5
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1956T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2279T>C
  hgvsp: ENSP00000324573.4:p.Met760Thr
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1182T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2246T>C
  hgvsp: ENSP00000463534.1:p.Met749Thr
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2230T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2021T>C
  hgvsp: ENSP00000368763.4:p.Met674Thr
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.299T>C
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2114T>C
  hgvsp: ENSP00000438536.2:p.Met705Thr
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met760Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

17-18151261-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 18151261
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 18151261
    reference: chr 17
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462314
  ensembl transcript: ENST00000578558
  gene symbol: FLII
  hgvsc: ENST00000578558.1:c.1931+1180G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000438536
  ensembl transcript: ENST00000545457
  gene symbol: FLII
  hgvsc: ENST00000545457.2:c.2112G>A
  hgvsp: ENST00000545457.2:c.2112G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463534
  ensembl transcript: ENST00000579294
  gene symbol: FLII
  hgvsc: ENST00000579294.1:c.2244G>A
  hgvsp: ENST00000579294.1:c.2244G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000463675
  ensembl transcript: ENST00000577485
  gene symbol: FLII
  hgvsc: ENST00000577485.1:c.218-1958G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000462293
  ensembl transcript: ENST00000578101
  gene symbol: FLII
  hgvsc: ENST00000578101.1:c.*2228G>A
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000368763
  ensembl transcript: ENST00000379450
  gene symbol: FLII
  hgvsc: ENST00000379450.4:c.2019G>A
  hgvsp: ENST00000379450.4:c.2019G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000177731
  ensembl protein: ENSP00000324573
  ensembl transcript: ENST00000327031
  gene symbol: FLII
  hgvsc: ENST00000327031.4:c.2277G>A
  hgvsp: ENST00000327031.4:c.2277G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3750
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177731
  ensembl transcript: ENST00000577402
  gene symbol: FLII
  hgvsc: ENST00000577402.1:n.297G>A
  variant of: http://identifiers.org/hgnc/3750
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu759Leu
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 163
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1234
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1744
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2400
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7303
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 9.75e1
variant carriers: 193

GenotypeQuality
all individuals: 500
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 189
allele frequency: 1.845703125e-2
allele num: 10240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551831160769708e-5
allele num: 64440
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11024
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: 8574
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.612330198537095e-4
allele num: 11484
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.361e1

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.354172e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 809
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4721
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10326
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2630
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18222
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.998401278976818e-4
allele num: 20016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2104
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2706
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.229e1

DP
type: SiteQuality
SIO_000300: 4.63069e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.221e0

VQSLOD
type: SiteQuality
SIO_000300: 9.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.52e-2

GenotypeQuality
all individuals: 4928
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3653
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5479
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24840
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.799846404915043e-5
allele num: 20834
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2922
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3874
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.15e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.96e-1

DP
type: SiteQuality
SIO_000300: 4.89838e5

FS
type: SiteQuality
SIO_000300: 3.484e0

MQRankSum
type: SiteQuality
SIO_000300: -3.46e-1

QD
type: SiteQuality
SIO_000300: 1.341e1

VQSLOD
type: SiteQuality
SIO_000300: 6.820000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3969
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10228
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5479
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20834
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3874
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.484e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.15e-2

DP
type: SiteQuality
SIO_000300: 4.89838e5

MQRankSum
type: SiteQuality
SIO_000300: -3.46e-1

QD
type: SiteQuality
SIO_000300: 1.341e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.820000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.96e-1

GenotypeQuality
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8232
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2199
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29762
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5171
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22232
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2468
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.395783421178726e-4
allele num: 4174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3208
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
type: SiteQuality
SIO_000300: 2.473e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.76e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 5.34531e5

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

GenotypeQuality
all individuals: 1861
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5171
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29762
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3357
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2199
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22232
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4174
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.76e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
type: SiteQuality
SIO_000300: 2.473e0

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

DP
type: SiteQuality
SIO_000300: 5.34531e5

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

GenotypeQuality
all individuals: 1447
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3681
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17311
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2899
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 189
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3020
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6972
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4310
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.707111060381235e-5
allele num: 35044
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.651800462504129e-4
allele num: 6054
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

DP
type: SiteQuality
SIO_000300: 7.8224e5

MQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

GenotypeQuality
all individuals: 82
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21106
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2655
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1342
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6808
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.605931099181738e-5
allele num: 38374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.871e1

QD
type: SiteQuality
SIO_000300: 9.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

DP
type: SiteQuality
SIO_000300: 8.38433e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.438e0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

GenotypeQuality
all individuals: 554
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 2394
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1588
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 184
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33152
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 1.484413656605641e-3
allele num: 4042
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.010672703751617e-4
allele num: 49472
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.051576e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

FS
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

QD
type: SiteQuality
SIO_000300: 1.137e1

GenotypeQuality
all individuals: 1274
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 243
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10539
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37068
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.881679963871745e-5
allele num: 53144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7004
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.576905591756326e-5
allele num: 13198
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e-1

FS
type: SiteQuality
SIO_000300: 1.291e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

DP
type: SiteQuality
SIO_000300: 1.130335e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.194e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

VQSLOD
type: SiteQuality
SIO_000300: -7.241e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

QD
type: SiteQuality
SIO_000300: 1.65e0

GenotypeQuality
all individuals: 720
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1032
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 37079
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1357
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.792243171553516e-5
allele num: 55796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7704
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 7.985094490284802e-4
allele num: 7514
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.74914089347079e-4
allele num: 14550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4762
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10528
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.386e-1

DP
type: SiteQuality
SIO_000300: 1.185476e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.37e-1

QD
type: SiteQuality
SIO_000300: 1.134e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.1e-2

MQ
type: SiteQuality
SIO_000300: 5.896e1

GenotypeQuality
all individuals: 353
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
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GenotypeQuality
all individuals: 7128
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variant carriers: 0

GenotypeQuality
all individuals: 38551
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 510
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variant carriers: 0

GenotypeQuality
all individuals: 338
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variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5094
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.509633945179517e-5
allele num: 56986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7798
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10686
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.214976e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

FS
type: SiteQuality
SIO_000300: 3.912e0

VQSLOD
type: SiteQuality
SIO_000300: -1.732e0

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

QD
type: SiteQuality
SIO_000300: 2.488e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.285e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeQuality
all individuals: 162
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
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variant carriers: 0

GenotypeQuality
all individuals: 39240
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 11

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 388
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variant carriers: 0

GenotypeQuality
all individuals: 1441
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variant carriers: 0

GenotypeQuality
all individuals: 1225
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variant carriers: 0

GenotypeQuality
all individuals: 658
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 3648
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5162
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.316191540898081e-5
allele num: 10734
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.27258844489692e-4
allele num: 7858
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.745078877565266e-4
allele num: 57304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7840
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.215113e6

FS
type: SiteQuality
SIO_000300: 6.434e0

QD
type: SiteQuality
SIO_000300: 1.422e1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.51e-1

GenotypeQuality
all individuals: 34593
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
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variant carriers: 0

GenotypeQuality
all individuals: 1745
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GenotypeQuality
all individuals: 1569
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variant carriers: 0

GenotypeQuality
all individuals: 1418
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variant carriers: 0

GenotypeQuality
all individuals: 173
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variant carriers: 0

GenotypeQuality
all individuals: 569
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variant carriers: 0

GenotypeQuality
all individuals: 2892
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.562395354636458e-5
allele num: 56142
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.147766323024055e-4
allele num: 4656
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.324152542372881e-4
allele num: 7552
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.30890052356021e-4
allele num: 7640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10528
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.92e1

VQSLOD
type: SiteQuality
SIO_000300: -7.564e1

MQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

FS
type: SiteQuality
SIO_000300: 1.2812e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

DP
type: SiteQuality
SIO_000300: 1.210622e6

QD
type: SiteQuality
SIO_000300: 1.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

GenotypeQuality
all individuals: 1366
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1231
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 867
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variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 40795
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variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.552271483305966e-5
allele num: 58464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.754820936639118e-4
allele num: 10890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5536
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.352432981832041e-5
allele num: 15742
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7992
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 1.165e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

DP
type: SiteQuality
SIO_000300: 1.254243e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.451e0

GenotypeQuality
all individuals: 580
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 863
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4016
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5731
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8136
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5442
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 5.073566717402334e-4
allele num: 15768
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58578
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.553e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.052e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e-1

FS
type: SiteQuality
SIO_000300: 8.134e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 1.259399e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
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GenotypeQuality
all individuals: 588
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variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 1.25e1
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GenotypeQuality
all individuals: 922
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4320
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GenotypeQuality
all individuals: 951
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GenotypeQuality
all individuals: 673
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GenotypeQuality
all individuals: 939
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variant carriers: 0

GenotypeQuality
all individuals: 422
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variant carriers: 0

GenotypeQuality
all individuals: 42712
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variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 9.75e1
variant carriers: 12

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15992
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.475288910745021e-3
allele num: 8134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59588
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.111e1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.97e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 1.106e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

DP
type: SiteQuality
SIO_000300: 1.287909e6

GenotypeQuality
all individuals: 43903
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
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variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.5e0
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GenotypeQuality
all individuals: 596
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4355
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variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 4.25e1
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GenotypeQuality
all individuals: 1092
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GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 185
bin: 5.75e1
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GenotypeQuality
all individuals: 370
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11064
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5784
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.240639041437844e-5
allele num: 16024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.038e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.093e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.347e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.32e-1

FS
type: SiteQuality
SIO_000300: 1.0056e1

MQ
type: SiteQuality
SIO_000300: 5.933e1

DP
type: SiteQuality
SIO_000300: 1.294904e6

GenotypeQuality
all individuals: 330
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4355
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 857
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.236746912810279e-5
allele num: 16034
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11066
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.288e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.57e-1

DP
type: SiteQuality
SIO_000300: 1.297102e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

MQRankSum
type: SiteQuality
SIO_000300: -1.463e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

QD
type: SiteQuality
SIO_000300: 1.496e1

GenotypeQuality
all individuals: 4701
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43324
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 1.75e1
variant carriers: 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: 8458
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.030160736861116e-5
allele num: 11074
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5826
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

MQRankSum
type: SiteQuality
SIO_000300: 2.26e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.167e0

DP
type: SiteQuality
SIO_000300: 1.301997e6

VQSLOD
type: SiteQuality
SIO_000300: -1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.77e-1

QD
type: SiteQuality
SIO_000300: 1.439e1

GenotypeQuality
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 492
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variant carriers: 0

GenotypeQuality
all individuals: 4365
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 175
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
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variant carriers: 0

GenotypeQuality
all individuals: 43324
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5826
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.030160736861116e-5
allele num: 11074
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.439e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.167e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.29e0

DP
type: SiteQuality
SIO_000300: 1.301997e6

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43670
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1019
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variant carriers: 0

GenotypeQuality
all individuals: 596
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variant carriers: 0

GenotypeQuality
all individuals: 961
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variant carriers: 0

GenotypeQuality
all individuals: 4610
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
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variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 704
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variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.160554413422641e-4
allele num: 60316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16096
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

QD
type: SiteQuality
SIO_000300: 1.289e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.925e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

FS
type: SiteQuality
SIO_000300: 4.074e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQRankSum
type: SiteQuality
SIO_000300: -1.206e0

DP
type: SiteQuality
SIO_000300: 1.306027e6

VQSLOD
type: SiteQuality
SIO_000300: -1.944e-1

GenotypeQuality
all individuals: 963
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
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variant carriers: 0

GenotypeQuality
all individuals: 349
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variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 854
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variant carriers: 0

GenotypeQuality
all individuals: 181
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variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 614
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variant carriers: 0

GenotypeQuality
all individuals: 4333
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
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variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4415
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5928
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.21713729308666e-4
allele num: 8216
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.644358206991811e-5
allele num: 60814
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.315886984715146e-4
allele num: 8636
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.85e-1

DP
type: SiteQuality
SIO_000300: 1.319312e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

QD
type: SiteQuality
SIO_000300: 1.211e1

FS
type: SiteQuality
SIO_000300: 8.824e0

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4011
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
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GenotypeQuality
all individuals: 985
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variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.134816159782115e-4
allele num: 8812
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5982
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.336259e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 3.368e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

QD
type: SiteQuality
SIO_000300: 3.76e0

VQSLOD
type: SiteQuality
SIO_000300: -1.481e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 688
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 771
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variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 532
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6080
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.675546668386763e-5
allele num: 62012
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

DP
type: SiteQuality
SIO_000300: 1.350135e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

VQSLOD
type: SiteQuality
SIO_000300: -5.051e-1

FS
type: SiteQuality
SIO_000300: 9.411e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

QD
type: SiteQuality
SIO_000300: 9.58e0

GenotypeQuality
all individuals: 111
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3230
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 383
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 339
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variant carriers: 0

GenotypeQuality
all individuals: 307
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 3

GenotypeQuality
all individuals: 69
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4776
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variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.772965921023324e-5
allele num: 62854
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 5.701e0

DP
type: SiteQuality
SIO_000300: 1.367402e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.496e0

VQSLOD
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

QD
type: SiteQuality
SIO_000300: 1.217e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-2

GenotypeQuality
all individuals: 574
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4830
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 5.75e1
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GenotypeQuality
all individuals: 816
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3028
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1060
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9366
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.585087496829825e-5
allele num: 63088
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.373981e6

VQSLOD
type: SiteQuality
SIO_000300: -3.34e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

FS
type: SiteQuality
SIO_000300: 5.474e0

QD
type: SiteQuality
SIO_000300: 1.721e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6210
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.049097775912715e-4
allele num: 9532
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11340
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.18e-1

DP
type: SiteQuality
SIO_000300: 1.384374e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

QD
type: SiteQuality
SIO_000300: 1.027e1

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: 12

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
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allele count: 5
allele frequency: 7.989773090444232e-4
allele num: 6258
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.09320339830085e-4
allele num: 64032
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.94e-1

DP
type: SiteQuality
SIO_000300: 1.394715e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 317
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64460
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.030869212022746e-4
allele num: 9848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

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

East Asian
type: Population
allele count: 21
allele frequency: 2.470007057163021e-3
allele num: 8502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.825261620832319e-4
allele num: 16436
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.403421e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

QD
type: SiteQuality
SIO_000300: 1.182e1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.444e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6302
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9872
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550051151688006e-5
allele num: 64514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.404777e6

QD
type: SiteQuality
SIO_000300: 1.073e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.95e-1

FS
type: SiteQuality
SIO_000300: 4.129e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64854
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.412469e6

MQRankSum
type: SiteQuality
SIO_000300: 9.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.583e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.46e-2

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

GenotypeQuality
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variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540832049306625e-5
allele num: 64900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
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: 882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.871e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.414059e6

MQRankSum
type: SiteQuality
SIO_000300: 7.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.093e-1

FS
type: SiteQuality
SIO_000300: 1.377e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 7.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.02e-1

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539361472861057e-5
allele num: 64962
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 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: 10024
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e-1

FS
type: SiteQuality
SIO_000300: 2.587e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.41416e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 344
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.601854969542992e-4
allele num: 65338
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.869719699960521e-5
allele num: 10132
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 6.678809957498482e-4
allele num: 16470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.84e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.423372e6

MQRankSum
type: SiteQuality
SIO_000300: 1.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.98e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 49612
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variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.838646202282565e-5
allele num: 10164
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

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: 8.44e-1

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.427651e6

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

QD
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SIO_000300: 1.588e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-1

ClippingRankSum
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SIO_000300: 1.45e0

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: 5

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65622
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

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

South Asian
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allele count: 6
allele frequency: 3.641660597232338e-4
allele num: 16476
num of homozygotes: 1

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

ClippingRankSum
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SIO_000300: -2.92e-1

BaseQRankSum
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SIO_000300: -1.624e0

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 1.43334e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.62e-2

FS
type: SiteQuality
SIO_000300: 1.1208e1

MQRankSum
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SIO_000300: 9.59e-1

QD
type: SiteQuality
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VQSLOD
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SIO_000300: -1.132e0

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

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

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

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

East Asian
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allele count: 3
allele frequency: 3.484320557491289e-4
allele num: 8610
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65722
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.35e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

DP
type: SiteQuality
SIO_000300: 1.435955e6

GenotypeQuality
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variant carriers: 18

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

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

Latino
type: Population
allele count: 18
allele frequency: 1.564673157162726e-3
allele num: 11504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.2e-2

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.151e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.335e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.438693e6

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

African
type: Population
allele count: 1
allele frequency: 9.742790335151988e-5
allele num: 10264
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.2e-2

QD
type: SiteQuality
SIO_000300: 1.335e1

MQRankSum
type: SiteQuality
SIO_000300: -2.61e-1

FS
type: SiteQuality
SIO_000300: 1.151e0

DP
type: SiteQuality
SIO_000300: 1.438693e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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: 6476
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.92169848071679e-4
allele num: 10268
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65802
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

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
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: 10270
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.518879674352198e-5
allele num: 65838
num of homozygotes: 0

QD
type: SiteQuality
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65838
num of homozygotes: 0

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

African
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allele count: 0
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InbreedingCoeff
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FS
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VQSLOD
type: SiteQuality
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BaseQRankSum
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QD
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DP
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ClippingRankSum
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MQRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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African
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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Other
type: Population
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Latino
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allele frequency: 8.680555555555556e-5
allele num: 11520
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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FS
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

East Asian
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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: 6500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516990291262136e-5
allele num: 65920
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.500000000000001e-3

DP
type: SiteQuality
SIO_000300: 1.442488e6

MQRankSum
type: SiteQuality
SIO_000300: 7.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.681e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.24e-1

GenotypeQuality
all individuals: 11
bin: 1.75e1
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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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 5314
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516300227445034e-5
allele num: 65950
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.699e1

VQSLOD
type: SiteQuality
SIO_000300: -1.808e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

QD
type: SiteQuality
SIO_000300: 1.63e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.442672e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 170
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66020
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.034e1

FS
type: SiteQuality
SIO_000300: 4.651e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.602e0

MQRankSum
type: SiteQuality
SIO_000300: -9.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

VQSLOD
type: SiteQuality
SIO_000300: 1.96e-1

DP
type: SiteQuality
SIO_000300: 1.446107e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514279657167086e-5
allele num: 66038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.446567e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.669e0

QD
type: SiteQuality
SIO_000300: 1.114e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

GenotypeQuality
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
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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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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
all individuals: 18
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GenotypeQuality
all individuals: 85
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.446757e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 5.685e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

QD
type: SiteQuality
SIO_000300: 1.307e1

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 88
bin: 9.75e1
variant carriers: 5

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.565441065214103e-5
allele num: 66090
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.75e-1

QD
type: SiteQuality
SIO_000300: 1.502e1

DP
type: SiteQuality
SIO_000300: 1.449406e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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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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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 60
allele frequency: 9.06590915959022e-4
allele num: 66182
num of homozygotes: 2

Latino
type: Population
allele count: 5
allele frequency: 4.337265787647467e-4
allele num: 11528
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.059975520195838e-4
allele num: 6536
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.14e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

VQSLOD
type: SiteQuality
SIO_000300: 5.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.454542e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.38e-1

QD
type: SiteQuality
SIO_000300: 1.444e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 151
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 124
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51391
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510984859931704e-5
allele num: 66182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.14e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.38e-1

DP
type: SiteQuality
SIO_000300: 1.454542e6

VQSLOD
type: SiteQuality
SIO_000300: 5.39e0

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.444e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

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: 86
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variant carriers: 1

GenotypeQuality
all individuals: 1132
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508750754375377e-5
allele num: 66280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.454606e6

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

FS
type: SiteQuality
SIO_000300: 1.162e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.831e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.72e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.65e-1

QD
type: SiteQuality
SIO_000300: 1.212e1

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 75
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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: 84
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GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66280
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.733402669440111e-4
allele num: 11538
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.72e-1

FS
type: SiteQuality
SIO_000300: 1.162e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.65e-1

DP
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SIO_000300: 1.454606e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

QD
type: SiteQuality
SIO_000300: 1.212e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.831e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

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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bin: 7.25e1
variant carriers: 0

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

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

South Asian
type: Population
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: 6556
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507340749449821e-5
allele num: 66342
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.6e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 5.158e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.502e0

DP
type: SiteQuality
SIO_000300: 1.456361e6

QD
type: SiteQuality
SIO_000300: 1.049e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.04e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66454
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
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: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

South Asian
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allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

MQ
type: SiteQuality
SIO_000300: 6.026e1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.54e-1

FS
type: SiteQuality
SIO_000300: 2.916e0

MQRankSum
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SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.109e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.017933441656135e-5
allele num: 66468
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.45e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.460617e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 6.22e-1

QD
type: SiteQuality
SIO_000300: 1.598e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504392827055001e-5
allele num: 66472
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.015e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.83e-1

DP
type: SiteQuality
SIO_000300: 1.461192e6

QD
type: SiteQuality
SIO_000300: 1.499e1

MQRankSum
type: SiteQuality
SIO_000300: 7.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 2.134e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e0

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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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.513178481165002e-5
allele num: 66472
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.461192e6

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e0

FS
type: SiteQuality
SIO_000300: 2.134e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
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
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504030802550836e-5
allele num: 66488
num of homozygotes: 0

DP
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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MQ
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ReadPosRankSum
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 3.832e0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

Latino
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allele frequency: 8.658008658008658e-5
allele num: 11550
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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QD
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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Other
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South Asian
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East Asian
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allele frequency: 2.313743637204998e-4
allele num: 8644
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Latino
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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allele frequency: 9.622786759045419e-5
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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BaseQRankSum
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FS
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VQSLOD
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QD
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MQ
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ClippingRankSum
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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South Asian
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Other
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MQ
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QD
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ReadPosRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Other
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Non-Finnish)
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East Asian
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Latino
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allele frequency: 2.593360995850622e-4
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European (Finnish)
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Other
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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MQ
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QD
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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African
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Other
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South Asian
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MQRankSum
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InbreedingCoeff
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Other
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East Asian
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Latino
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European (Non-Finnish)
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FS
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VQSLOD
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DP
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ClippingRankSum
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MQRankSum
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QD
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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East Asian
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MQ
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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DP
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