2-216271076-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271076
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271076
    reference: chr 2
allele count: 2
allele frequency: 1.648288252649623e-5
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2871C>T
  hgvsp: ENST00000323926.6:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2871C>T
  hgvsp: ENST00000357867.4:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2871C>T
  hgvsp: ENST00000359671.1:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2871C>T
  hgvsp: ENST00000336916.4:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2871C>T
  hgvsp: ENST00000345488.5:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2871C>T
  hgvsp: ENST00000354785.4:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2871C>T
  hgvsp: ENST00000446046.1:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2871C>T
  hgvsp: ENST00000357009.2:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2871C>T
  hgvsp: ENST00000432072.2:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2871C>T
  hgvsp: ENST00000356005.4:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2871C>T
  hgvsp: ENST00000346544.3:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2871C>T
  hgvsp: ENST00000443816.1:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2871C>T
  hgvsp: ENST00000421182.1:c.2871C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser957Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

2-216271081-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271081
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271081
    reference: chr 2
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2866A>G
  hgvsp: ENSP00000346839.4:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2866A>G
  hgvsp: ENSP00000323534.6:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2866A>G
  hgvsp: ENSP00000394423.1:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2866A>G
  hgvsp: ENSP00000338200.4:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2866A>G
  hgvsp: ENSP00000348285.4:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2866A>G
  hgvsp: ENSP00000399538.2:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2866A>G
  hgvsp: ENSP00000350534.4:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2866A>G
  hgvsp: ENSP00000265312.6:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2866A>G
  hgvsp: ENSP00000349509.2:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2866A>G
  hgvsp: ENSP00000273049.7:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2866A>G
  hgvsp: ENSP00000410422.1:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2866A>G
  hgvsp: ENSP00000415018.1:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2866A>G
  hgvsp: ENSP00000352696.1:p.Ile956Val
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29339
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile956Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

2-216271082-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271082
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271082
    reference: chr 2
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2865C>T
  hgvsp: ENST00000356005.4:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2865C>T
  hgvsp: ENST00000357009.2:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2865C>T
  hgvsp: ENST00000345488.5:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2865C>T
  hgvsp: ENST00000357867.4:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2865C>T
  hgvsp: ENST00000346544.3:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2865C>T
  hgvsp: ENST00000354785.4:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2865C>T
  hgvsp: ENST00000432072.2:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2865C>T
  hgvsp: ENST00000336916.4:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2865C>T
  hgvsp: ENST00000359671.1:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2865C>T
  hgvsp: ENST00000446046.1:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2865C>T
  hgvsp: ENST00000443816.1:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2865C>T
  hgvsp: ENST00000421182.1:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2865C>T
  hgvsp: ENST00000323926.6:c.2865C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro955Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

2-216271096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271096
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271096
    reference: chr 2
allele count: 3
allele frequency: 2.472880741204788e-5
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2851G>A
  hgvsp: ENSP00000399538.2:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2851G>A
  hgvsp: ENSP00000349509.2:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2851G>A
  hgvsp: ENSP00000323534.6:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2851G>A
  hgvsp: ENSP00000273049.7:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2851G>A
  hgvsp: ENSP00000348285.4:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2851G>A
  hgvsp: ENSP00000338200.4:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2851G>A
  hgvsp: ENSP00000415018.1:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2851G>A
  hgvsp: ENSP00000346839.4:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2851G>A
  hgvsp: ENSP00000394423.1:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2851G>A
  hgvsp: ENSP00000265312.6:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2851G>A
  hgvsp: ENSP00000410422.1:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2851G>A
  hgvsp: ENSP00000352696.1:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2851G>A
  hgvsp: ENSP00000350534.4:p.Gly951Arg
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly951Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

2-216271097-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271097
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271097
    reference: chr 2
allele count: 11
allele frequency: 9.067378868061394e-5
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2850C>T
  hgvsp: ENST00000345488.5:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2850C>T
  hgvsp: ENST00000359671.1:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2850C>T
  hgvsp: ENST00000357009.2:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2850C>T
  hgvsp: ENST00000432072.2:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2850C>T
  hgvsp: ENST00000357867.4:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2850C>T
  hgvsp: ENST00000323926.6:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2850C>T
  hgvsp: ENST00000336916.4:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2850C>T
  hgvsp: ENST00000356005.4:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2850C>T
  hgvsp: ENST00000346544.3:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2850C>T
  hgvsp: ENST00000443816.1:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2850C>T
  hgvsp: ENST00000354785.4:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2850C>T
  hgvsp: ENST00000446046.1:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2850C>T
  hgvsp: ENST00000421182.1:c.2850C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8721
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His950His
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

2-216271099-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271099
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271099
    reference: chr 2
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2848C>T
  hgvsp: ENSP00000399538.2:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2848C>T
  hgvsp: ENSP00000348285.4:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2848C>T
  hgvsp: ENSP00000346839.4:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2848C>T
  hgvsp: ENSP00000415018.1:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2848C>T
  hgvsp: ENSP00000273049.7:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2848C>T
  hgvsp: ENSP00000338200.4:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2848C>T
  hgvsp: ENSP00000349509.2:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2848C>T
  hgvsp: ENSP00000265312.6:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2848C>T
  hgvsp: ENSP00000323534.6:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2848C>T
  hgvsp: ENSP00000394423.1:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2848C>T
  hgvsp: ENSP00000352696.1:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2848C>T
  hgvsp: ENSP00000350534.4:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2848C>T
  hgvsp: ENSP00000410422.1:p.His950Tyr
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His950Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-216271102-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271102
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271102
    reference: chr 2
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2845G>C
  hgvsp: ENSP00000399538.2:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2845G>C
  hgvsp: ENSP00000350534.4:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2845G>C
  hgvsp: ENSP00000273049.7:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2845G>C
  hgvsp: ENSP00000352696.1:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2845G>C
  hgvsp: ENSP00000349509.2:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2845G>C
  hgvsp: ENSP00000265312.6:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2845G>C
  hgvsp: ENSP00000415018.1:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2845G>C
  hgvsp: ENSP00000348285.4:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2845G>C
  hgvsp: ENSP00000410422.1:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2845G>C
  hgvsp: ENSP00000394423.1:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2845G>C
  hgvsp: ENSP00000338200.4:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2845G>C
  hgvsp: ENSP00000323534.6:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2845G>C
  hgvsp: ENSP00000346839.4:p.Glu949Gln
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu949Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ

2-216271102-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271102
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271102
    reference: chr 2
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2845G>A
  hgvsp: ENSP00000338200.4:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2845G>A
  hgvsp: ENSP00000348285.4:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2845G>A
  hgvsp: ENSP00000415018.1:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2845G>A
  hgvsp: ENSP00000410422.1:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2845G>A
  hgvsp: ENSP00000273049.7:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2845G>A
  hgvsp: ENSP00000399538.2:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2845G>A
  hgvsp: ENSP00000352696.1:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2845G>A
  hgvsp: ENSP00000350534.4:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2845G>A
  hgvsp: ENSP00000346839.4:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2845G>A
  hgvsp: ENSP00000349509.2:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2845G>A
  hgvsp: ENSP00000265312.6:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2845G>A
  hgvsp: ENSP00000394423.1:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2845G>A
  hgvsp: ENSP00000323534.6:p.Glu949Lys
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu949Lys
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ

2-216271112-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271112
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271112
    reference: chr 2
allele count: 2
allele frequency: 1.648723063986942e-5
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2835C>T
  hgvsp: ENST00000336916.4:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2835C>T
  hgvsp: ENST00000421182.1:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2835C>T
  hgvsp: ENST00000357867.4:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2835C>T
  hgvsp: ENST00000446046.1:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2835C>T
  hgvsp: ENST00000354785.4:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2835C>T
  hgvsp: ENST00000359671.1:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2835C>T
  hgvsp: ENST00000356005.4:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2835C>T
  hgvsp: ENST00000357009.2:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2835C>T
  hgvsp: ENST00000443816.1:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2835C>T
  hgvsp: ENST00000346544.3:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2835C>T
  hgvsp: ENST00000345488.5:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2835C>T
  hgvsp: ENST00000432072.2:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2835C>T
  hgvsp: ENST00000323926.6:c.2835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn945Asn
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

2-216271117-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271117
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271117
    reference: chr 2
allele count: 2
allele frequency: 1.649022129876983e-5
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2830G>A
  hgvsp: ENSP00000394423.1:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2830G>A
  hgvsp: ENSP00000415018.1:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2830G>A
  hgvsp: ENSP00000346839.4:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2830G>A
  hgvsp: ENSP00000410422.1:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2830G>A
  hgvsp: ENSP00000399538.2:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2830G>A
  hgvsp: ENSP00000350534.4:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2830G>A
  hgvsp: ENSP00000338200.4:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2830G>A
  hgvsp: ENSP00000349509.2:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2830G>A
  hgvsp: ENSP00000348285.4:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2830G>A
  hgvsp: ENSP00000265312.6:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2830G>A
  hgvsp: ENSP00000323534.6:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2830G>A
  hgvsp: ENSP00000352696.1:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2830G>A
  hgvsp: ENSP00000273049.7:p.Val944Ile
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val944Ile
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

2-216271118-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271118
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271118
    reference: chr 2
allele count: 23
allele frequency: 1.896531820505632e-4
allele num: 121274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2829C>T
  hgvsp: ENST00000356005.4:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2829C>T
  hgvsp: ENST00000323926.6:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2829C>T
  hgvsp: ENST00000443816.1:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2829C>T
  hgvsp: ENST00000357867.4:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2829C>T
  hgvsp: ENST00000345488.5:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2829C>T
  hgvsp: ENST00000359671.1:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2829C>T
  hgvsp: ENST00000421182.1:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2829C>T
  hgvsp: ENST00000354785.4:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2829C>T
  hgvsp: ENST00000357009.2:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2829C>T
  hgvsp: ENST00000336916.4:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2829C>T
  hgvsp: ENST00000432072.2:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2829C>T
  hgvsp: ENST00000446046.1:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2829C>T
  hgvsp: ENST00000346544.3:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29222
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8610
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14441
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro943Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

2-216271123-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271123
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271123
    reference: chr 2
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2824A>G
  hgvsp: ENSP00000323534.6:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2824A>G
  hgvsp: ENSP00000350534.4:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2824A>G
  hgvsp: ENSP00000346839.4:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2824A>G
  hgvsp: ENSP00000399538.2:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2824A>G
  hgvsp: ENSP00000415018.1:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2824A>G
  hgvsp: ENSP00000273049.7:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2824A>G
  hgvsp: ENSP00000352696.1:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2824A>G
  hgvsp: ENSP00000348285.4:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2824A>G
  hgvsp: ENSP00000338200.4:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2824A>G
  hgvsp: ENSP00000349509.2:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2824A>G
  hgvsp: ENSP00000394423.1:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2824A>G
  hgvsp: ENSP00000265312.6:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2824A>G
  hgvsp: ENSP00000410422.1:p.Ile942Val
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile942Val
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

2-216271126-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271126
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271126
    reference: chr 2
allele count: 9
allele frequency: 7.422680412371133e-5
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2821G>A
  hgvsp: ENSP00000346839.4:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2821G>A
  hgvsp: ENSP00000273049.7:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2821G>A
  hgvsp: ENSP00000348285.4:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2821G>A
  hgvsp: ENSP00000399538.2:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2821G>A
  hgvsp: ENSP00000323534.6:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2821G>A
  hgvsp: ENSP00000352696.1:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2821G>A
  hgvsp: ENSP00000410422.1:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2821G>A
  hgvsp: ENSP00000349509.2:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2821G>A
  hgvsp: ENSP00000265312.6:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2821G>A
  hgvsp: ENSP00000415018.1:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2821G>A
  hgvsp: ENSP00000394423.1:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2821G>A
  hgvsp: ENSP00000338200.4:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2821G>A
  hgvsp: ENSP00000350534.4:p.Val941Met
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val941Met
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

2-216271129-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271129
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271129
    reference: chr 2
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2818G>A
  hgvsp: ENSP00000399538.2:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2818G>A
  hgvsp: ENSP00000394423.1:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2818G>A
  hgvsp: ENSP00000350534.4:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2818G>A
  hgvsp: ENSP00000346839.4:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2818G>A
  hgvsp: ENSP00000273049.7:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2818G>A
  hgvsp: ENSP00000323534.6:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2818G>A
  hgvsp: ENSP00000415018.1:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2818G>A
  hgvsp: ENSP00000265312.6:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2818G>A
  hgvsp: ENSP00000348285.4:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2818G>A
  hgvsp: ENSP00000349509.2:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2818G>A
  hgvsp: ENSP00000338200.4:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2818G>A
  hgvsp: ENSP00000352696.1:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2818G>A
  hgvsp: ENSP00000410422.1:p.Asp940Asn
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp940Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

2-216271134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271134
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271134
    reference: chr 2
allele count: 4
allele frequency: 3.300874731803928e-5
allele num: 121180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2813G>A
  hgvsp: ENSP00000349509.2:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2813G>A
  hgvsp: ENSP00000323534.6:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2813G>A
  hgvsp: ENSP00000415018.1:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2813G>A
  hgvsp: ENSP00000273049.7:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2813G>A
  hgvsp: ENSP00000346839.4:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2813G>A
  hgvsp: ENSP00000399538.2:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2813G>A
  hgvsp: ENSP00000352696.1:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2813G>A
  hgvsp: ENSP00000265312.6:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2813G>A
  hgvsp: ENSP00000348285.4:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2813G>A
  hgvsp: ENSP00000350534.4:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2813G>A
  hgvsp: ENSP00000410422.1:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2813G>A
  hgvsp: ENSP00000338200.4:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2813G>A
  hgvsp: ENSP00000394423.1:p.Arg938His
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg938His
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

2-216271135-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271135
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271135
    reference: chr 2
allele count: 2
allele frequency: 1.650491846570278e-5
allele num: 121176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2812C>T
  hgvsp: ENSP00000399538.2:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2812C>T
  hgvsp: ENSP00000348285.4:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2812C>T
  hgvsp: ENSP00000346839.4:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2812C>T
  hgvsp: ENSP00000323534.6:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2812C>T
  hgvsp: ENSP00000415018.1:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2812C>T
  hgvsp: ENSP00000349509.2:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2812C>T
  hgvsp: ENSP00000410422.1:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2812C>T
  hgvsp: ENSP00000350534.4:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2812C>T
  hgvsp: ENSP00000394423.1:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2812C>T
  hgvsp: ENSP00000265312.6:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2812C>T
  hgvsp: ENSP00000338200.4:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2812C>T
  hgvsp: ENSP00000352696.1:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2812C>T
  hgvsp: ENSP00000273049.7:p.Arg938Cys
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg938Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

2-216271139-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271139
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271139
    reference: chr 2
allele count: 82
allele frequency: 6.768021921788078e-4
allele num: 121158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2808C>G
  hgvsp: ENST00000356005.4:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2808C>G
  hgvsp: ENST00000354785.4:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2808C>G
  hgvsp: ENST00000357867.4:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2808C>G
  hgvsp: ENST00000345488.5:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2808C>G
  hgvsp: ENST00000446046.1:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2808C>G
  hgvsp: ENST00000443816.1:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2808C>G
  hgvsp: ENST00000346544.3:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2808C>G
  hgvsp: ENST00000432072.2:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2808C>G
  hgvsp: ENST00000421182.1:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2808C>G
  hgvsp: ENST00000357009.2:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2808C>G
  hgvsp: ENST00000359671.1:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2808C>G
  hgvsp: ENST00000323926.6:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2808C>G
  hgvsp: ENST00000336916.4:c.2808C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29209
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8334
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly936Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

2-216271141-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271141
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271141
    reference: chr 2
allele count: 3
allele frequency: 2.476228209191759e-5
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2806G>A
  hgvsp: ENSP00000415018.1:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2806G>A
  hgvsp: ENSP00000348285.4:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2806G>A
  hgvsp: ENSP00000410422.1:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2806G>A
  hgvsp: ENSP00000338200.4:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2806G>A
  hgvsp: ENSP00000265312.6:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2806G>A
  hgvsp: ENSP00000346839.4:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2806G>A
  hgvsp: ENSP00000273049.7:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2806G>A
  hgvsp: ENSP00000323534.6:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2806G>A
  hgvsp: ENSP00000349509.2:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2806G>A
  hgvsp: ENSP00000399538.2:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2806G>A
  hgvsp: ENSP00000394423.1:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2806G>A
  hgvsp: ENSP00000350534.4:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2806G>A
  hgvsp: ENSP00000352696.1:p.Gly936Ser
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14710
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly936Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

2-216271142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271142
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271142
    reference: chr 2
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2805C>T
  hgvsp: ENST00000354785.4:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2805C>T
  hgvsp: ENST00000357867.4:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2805C>T
  hgvsp: ENST00000443816.1:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2805C>T
  hgvsp: ENST00000359671.1:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2805C>T
  hgvsp: ENST00000345488.5:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2805C>T
  hgvsp: ENST00000346544.3:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2805C>T
  hgvsp: ENST00000446046.1:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2805C>T
  hgvsp: ENST00000356005.4:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2805C>T
  hgvsp: ENST00000421182.1:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2805C>T
  hgvsp: ENST00000336916.4:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2805C>T
  hgvsp: ENST00000323926.6:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2805C>T
  hgvsp: ENST00000432072.2:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2805C>T
  hgvsp: ENST00000357009.2:c.2805C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8300
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr935Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

2-216271143-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271143
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271143
    reference: chr 2
allele count: 2
allele frequency: 1.650818806127839e-5
allele num: 121152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2804C>T
  hgvsp: ENSP00000273049.7:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2804C>T
  hgvsp: ENSP00000415018.1:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2804C>T
  hgvsp: ENSP00000349509.2:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2804C>T
  hgvsp: ENSP00000265312.6:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2804C>T
  hgvsp: ENSP00000394423.1:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2804C>T
  hgvsp: ENSP00000338200.4:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2804C>T
  hgvsp: ENSP00000352696.1:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2804C>T
  hgvsp: ENSP00000350534.4:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2804C>T
  hgvsp: ENSP00000346839.4:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2804C>T
  hgvsp: ENSP00000410422.1:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2804C>T
  hgvsp: ENSP00000348285.4:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2804C>T
  hgvsp: ENSP00000323534.6:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2804C>T
  hgvsp: ENSP00000399538.2:p.Thr935Ile
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29221
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr935Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

2-216271156-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271156
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271156
    reference: chr 2
allele count: 3
allele frequency: 2.479953707530793e-5
allele num: 120970
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2791G>A
  hgvsp: ENSP00000415018.1:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2791G>A
  hgvsp: ENSP00000399538.2:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2791G>A
  hgvsp: ENSP00000265312.6:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2791G>A
  hgvsp: ENSP00000338200.4:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2791G>A
  hgvsp: ENSP00000273049.7:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2791G>A
  hgvsp: ENSP00000350534.4:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2791G>A
  hgvsp: ENSP00000349509.2:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2791G>A
  hgvsp: ENSP00000348285.4:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2791G>A
  hgvsp: ENSP00000352696.1:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2791G>A
  hgvsp: ENSP00000323534.6:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2791G>A
  hgvsp: ENSP00000346839.4:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2791G>A
  hgvsp: ENSP00000410422.1:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2791G>A
  hgvsp: ENSP00000394423.1:p.Glu931Lys
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8060
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu931Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

2-216271156-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271156
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271156
    reference: chr 2
allele count: 1
allele frequency: 8.266512358435975e-6
allele num: 120970
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2791G>C
  hgvsp: ENSP00000338200.4:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2791G>C
  hgvsp: ENSP00000352696.1:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2791G>C
  hgvsp: ENSP00000350534.4:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2791G>C
  hgvsp: ENSP00000349509.2:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2791G>C
  hgvsp: ENSP00000346839.4:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2791G>C
  hgvsp: ENSP00000273049.7:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2791G>C
  hgvsp: ENSP00000265312.6:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2791G>C
  hgvsp: ENSP00000399538.2:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2791G>C
  hgvsp: ENSP00000348285.4:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2791G>C
  hgvsp: ENSP00000394423.1:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2791G>C
  hgvsp: ENSP00000323534.6:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2791G>C
  hgvsp: ENSP00000410422.1:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2791G>C
  hgvsp: ENSP00000415018.1:p.Glu931Gln
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu931Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

2-216271157-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271157
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271157
    reference: chr 2
allele count: 1
allele frequency: 8.265555775970376e-6
allele num: 120984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2790T>C
  hgvsp: ENST00000446046.1:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2790T>C
  hgvsp: ENST00000357867.4:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2790T>C
  hgvsp: ENST00000346544.3:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2790T>C
  hgvsp: ENST00000432072.2:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2790T>C
  hgvsp: ENST00000421182.1:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2790T>C
  hgvsp: ENST00000359671.1:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2790T>C
  hgvsp: ENST00000357009.2:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2790T>C
  hgvsp: ENST00000345488.5:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2790T>C
  hgvsp: ENST00000354785.4:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2790T>C
  hgvsp: ENST00000323926.6:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2790T>C
  hgvsp: ENST00000356005.4:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2790T>C
  hgvsp: ENST00000443816.1:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2790T>C
  hgvsp: ENST00000336916.4:c.2790T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28954
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro930Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-216271160-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271160
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271160
    reference: chr 2
allele count: 6
allele frequency: 4.961055712655653e-5
allele num: 120942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2787G>A
  hgvsp: ENST00000336916.4:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2787G>A
  hgvsp: ENST00000356005.4:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2787G>A
  hgvsp: ENST00000432072.2:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2787G>A
  hgvsp: ENST00000354785.4:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2787G>A
  hgvsp: ENST00000421182.1:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2787G>A
  hgvsp: ENST00000357009.2:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2787G>A
  hgvsp: ENST00000443816.1:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2787G>A
  hgvsp: ENST00000323926.6:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2787G>A
  hgvsp: ENST00000345488.5:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2787G>A
  hgvsp: ENST00000357867.4:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2787G>A
  hgvsp: ENST00000446046.1:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2787G>A
  hgvsp: ENST00000346544.3:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2787G>A
  hgvsp: ENST00000359671.1:c.2787G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro929Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

2-216271161-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271161
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271161
    reference: chr 2
allele count: 2
allele frequency: 1.654341820106871e-5
allele num: 120894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2786C>T
  hgvsp: ENSP00000265312.6:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2786C>T
  hgvsp: ENSP00000348285.4:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2786C>T
  hgvsp: ENSP00000273049.7:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2786C>T
  hgvsp: ENSP00000415018.1:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2786C>T
  hgvsp: ENSP00000399538.2:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2786C>T
  hgvsp: ENSP00000410422.1:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2786C>T
  hgvsp: ENSP00000346839.4:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2786C>T
  hgvsp: ENSP00000350534.4:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2786C>T
  hgvsp: ENSP00000394423.1:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2786C>T
  hgvsp: ENSP00000349509.2:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2786C>T
  hgvsp: ENSP00000352696.1:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2786C>T
  hgvsp: ENSP00000338200.4:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2786C>T
  hgvsp: ENSP00000323534.6:p.Pro929Leu
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro929Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-216271163-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271163
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271163
    reference: chr 2
allele count: 1
allele frequency: 8.271709100534353e-6
allele num: 120894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2784A>T
  hgvsp: ENST00000346544.3:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2784A>T
  hgvsp: ENST00000357009.2:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2784A>T
  hgvsp: ENST00000421182.1:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2784A>T
  hgvsp: ENST00000443816.1:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2784A>T
  hgvsp: ENST00000432072.2:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2784A>T
  hgvsp: ENST00000357867.4:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2784A>T
  hgvsp: ENST00000356005.4:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2784A>T
  hgvsp: ENST00000359671.1:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2784A>T
  hgvsp: ENST00000336916.4:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2784A>T
  hgvsp: ENST00000354785.4:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2784A>T
  hgvsp: ENST00000345488.5:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2784A>T
  hgvsp: ENST00000323926.6:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2784A>T
  hgvsp: ENST00000446046.1:c.2784A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr928Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

2-216271170-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271170
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271170
    reference: chr 2
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2777T>C
  hgvsp: ENSP00000346839.4:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2777T>C
  hgvsp: ENSP00000338200.4:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2777T>C
  hgvsp: ENSP00000348285.4:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2777T>C
  hgvsp: ENSP00000349509.2:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2777T>C
  hgvsp: ENSP00000352696.1:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2777T>C
  hgvsp: ENSP00000265312.6:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2777T>C
  hgvsp: ENSP00000399538.2:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2777T>C
  hgvsp: ENSP00000350534.4:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2777T>C
  hgvsp: ENSP00000410422.1:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2777T>C
  hgvsp: ENSP00000394423.1:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2777T>C
  hgvsp: ENSP00000415018.1:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2777T>C
  hgvsp: ENSP00000273049.7:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2777T>C
  hgvsp: ENSP00000323534.6:p.Met926Thr
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met926Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

2-216271175-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271175
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271175
    reference: chr 2
allele count: 12
allele frequency: 9.947774185525989e-5
allele num: 120630
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2772C>T
  hgvsp: ENST00000357009.2:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2772C>T
  hgvsp: ENST00000356005.4:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2772C>T
  hgvsp: ENST00000336916.4:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2772C>T
  hgvsp: ENST00000354785.4:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2772C>T
  hgvsp: ENST00000446046.1:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2772C>T
  hgvsp: ENST00000357867.4:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2772C>T
  hgvsp: ENST00000443816.1:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2772C>T
  hgvsp: ENST00000359671.1:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2772C>T
  hgvsp: ENST00000432072.2:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2772C>T
  hgvsp: ENST00000421182.1:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2772C>T
  hgvsp: ENST00000345488.5:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2772C>T
  hgvsp: ENST00000323926.6:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2772C>T
  hgvsp: ENST00000346544.3:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28332
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr924Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

2-216271176-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271176
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271176
    reference: chr 2
allele count: 1
allele frequency: 8.292836647703714e-6
allele num: 120586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2771C>T
  hgvsp: ENSP00000265312.6:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2771C>T
  hgvsp: ENSP00000350534.4:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2771C>T
  hgvsp: ENSP00000410422.1:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2771C>T
  hgvsp: ENSP00000273049.7:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2771C>T
  hgvsp: ENSP00000415018.1:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2771C>T
  hgvsp: ENSP00000348285.4:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2771C>T
  hgvsp: ENSP00000399538.2:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2771C>T
  hgvsp: ENSP00000352696.1:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2771C>T
  hgvsp: ENSP00000346839.4:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2771C>T
  hgvsp: ENSP00000323534.6:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2771C>T
  hgvsp: ENSP00000349509.2:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2771C>T
  hgvsp: ENSP00000338200.4:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2771C>T
  hgvsp: ENSP00000394423.1:p.Thr924Ile
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr924Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

2-216271183-TCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271183
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271181
    reference: chr 2
allele count: 1
allele frequency: 8.314072398942449e-6
allele num: 120278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2762_2763delTG
  hgvsp: ENSP00000349509.2:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2762_2763delTG
  hgvsp: ENSP00000350534.4:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2762_2763delTG
  hgvsp: ENSP00000348285.4:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2762_2763delTG
  hgvsp: ENSP00000273049.7:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2762_2763delTG
  hgvsp: ENSP00000399538.2:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2762_2763delTG
  hgvsp: ENSP00000415018.1:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2762_2763delTG
  hgvsp: ENSP00000265312.6:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2762_2763delTG
  hgvsp: ENSP00000410422.1:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2762_2763delTG
  hgvsp: ENSP00000338200.4:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2762_2763delTG
  hgvsp: ENSP00000394423.1:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2762_2763delTG
  hgvsp: ENSP00000323534.6:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2762_2763delTG
  hgvsp: ENSP00000352696.1:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2762_2763delTG
  hgvsp: ENSP00000346839.4:p.Val921GlufsTer10
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val921GlufsTer10
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: TCA
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-216271187-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271187
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271187
    reference: chr 2
allele count: 1
allele frequency: 8.316976612661764e-6
allele num: 120236
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2760C>T
  hgvsp: ENST00000354785.4:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2760C>T
  hgvsp: ENST00000346544.3:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2760C>T
  hgvsp: ENST00000357009.2:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2760C>T
  hgvsp: ENST00000357867.4:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2760C>T
  hgvsp: ENST00000323926.6:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2760C>T
  hgvsp: ENST00000443816.1:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2760C>T
  hgvsp: ENST00000336916.4:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2760C>T
  hgvsp: ENST00000345488.5:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2760C>T
  hgvsp: ENST00000421182.1:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2760C>T
  hgvsp: ENST00000432072.2:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2760C>T
  hgvsp: ENST00000446046.1:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2760C>T
  hgvsp: ENST00000356005.4:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2760C>T
  hgvsp: ENST00000359671.1:c.2760C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp920Asp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP

2-216271197-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271197
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271197
    reference: chr 2
allele count: 1
allele frequency: 8.34278849362611e-6
allele num: 119864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2750A>C
  hgvsp: ENSP00000348285.4:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2750A>C
  hgvsp: ENSP00000399538.2:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2750A>C
  hgvsp: ENSP00000352696.1:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2750A>C
  hgvsp: ENSP00000349509.2:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2750A>C
  hgvsp: ENSP00000265312.6:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2750A>C
  hgvsp: ENSP00000346839.4:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2750A>C
  hgvsp: ENSP00000350534.4:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2750A>C
  hgvsp: ENSP00000410422.1:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2750A>C
  hgvsp: ENSP00000394423.1:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2750A>C
  hgvsp: ENSP00000338200.4:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2750A>C
  hgvsp: ENSP00000323534.6:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2750A>C
  hgvsp: ENSP00000273049.7:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2750A>C
  hgvsp: ENSP00000415018.1:p.Glu917Ala
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16434
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu917Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

2-216271202-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271202
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271202
    reference: chr 2
allele count: 1
allele frequency: 8.36344172353807e-6
allele num: 119568
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2745T>C
  hgvsp: ENST00000356005.4:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2745T>C
  hgvsp: ENST00000346544.3:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2745T>C
  hgvsp: ENST00000357009.2:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2745T>C
  hgvsp: ENST00000336916.4:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2745T>C
  hgvsp: ENST00000323926.6:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2745T>C
  hgvsp: ENST00000345488.5:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2745T>C
  hgvsp: ENST00000359671.1:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2745T>C
  hgvsp: ENST00000443816.1:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2745T>C
  hgvsp: ENST00000421182.1:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2745T>C
  hgvsp: ENST00000354785.4:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2745T>C
  hgvsp: ENST00000446046.1:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2745T>C
  hgvsp: ENST00000357867.4:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2745T>C
  hgvsp: ENST00000432072.2:c.2745T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe915Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

2-216271224-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271224
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271224
    reference: chr 2
allele count: 1
allele frequency: 8.553588230262596e-6
allele num: 116910
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2723C>A
  hgvsp: ENSP00000394423.1:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2723C>A
  hgvsp: ENSP00000273049.7:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2723C>A
  hgvsp: ENSP00000348285.4:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2723C>A
  hgvsp: ENSP00000323534.6:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2723C>A
  hgvsp: ENSP00000415018.1:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2723C>A
  hgvsp: ENSP00000399538.2:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2723C>A
  hgvsp: ENSP00000265312.6:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2723C>A
  hgvsp: ENSP00000346839.4:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2723C>A
  hgvsp: ENSP00000352696.1:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2723C>A
  hgvsp: ENSP00000349509.2:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2723C>A
  hgvsp: ENSP00000350534.4:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2723C>A
  hgvsp: ENSP00000338200.4:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2723C>A
  hgvsp: ENSP00000410422.1:p.Pro908His
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3941
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro908His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/2-216271226-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271226
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271226
    reference: chr 2
allele count: 4
allele frequency: 3.432945982594964e-5
allele num: 116518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2721G>T
  hgvsp: ENST00000443816.1:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2721G>T
  hgvsp: ENST00000345488.5:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2721G>T
  hgvsp: ENST00000357867.4:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2721G>T
  hgvsp: ENST00000354785.4:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2721G>T
  hgvsp: ENST00000432072.2:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2721G>T
  hgvsp: ENST00000446046.1:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2721G>T
  hgvsp: ENST00000346544.3:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2721G>T
  hgvsp: ENST00000356005.4:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2721G>T
  hgvsp: ENST00000421182.1:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2721G>T
  hgvsp: ENST00000336916.4:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2721G>T
  hgvsp: ENST00000359671.1:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2721G>T
  hgvsp: ENST00000323926.6:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2721G>T
  hgvsp: ENST00000357009.2:c.2721G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val907Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

2-216271226-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271226
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271226
    reference: chr 2
allele count: 1
allele frequency: 8.58236495648741e-6
allele num: 116518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2721G>A
  hgvsp: ENST00000345488.5:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2721G>A
  hgvsp: ENST00000443816.1:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2721G>A
  hgvsp: ENST00000354785.4:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2721G>A
  hgvsp: ENST00000432072.2:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2721G>A
  hgvsp: ENST00000421182.1:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2721G>A
  hgvsp: ENST00000446046.1:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2721G>A
  hgvsp: ENST00000323926.6:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2721G>A
  hgvsp: ENST00000356005.4:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2721G>A
  hgvsp: ENST00000346544.3:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2721G>A
  hgvsp: ENST00000357009.2:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2721G>A
  hgvsp: ENST00000357867.4:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2721G>A
  hgvsp: ENST00000359671.1:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2721G>A
  hgvsp: ENST00000336916.4:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val907Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

2-216271228-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271228
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271228
    reference: chr 2
allele count: 1
allele frequency: 8.617718028266114e-6
allele num: 116040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2719G>A
  hgvsp: ENSP00000399538.2:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2719G>A
  hgvsp: ENSP00000350534.4:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2719G>A
  hgvsp: ENSP00000415018.1:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2719G>A
  hgvsp: ENSP00000394423.1:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2719G>A
  hgvsp: ENSP00000348285.4:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2719G>A
  hgvsp: ENSP00000352696.1:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2719G>A
  hgvsp: ENSP00000346839.4:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2719G>A
  hgvsp: ENSP00000349509.2:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2719G>A
  hgvsp: ENSP00000323534.6:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2719G>A
  hgvsp: ENSP00000338200.4:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2719G>A
  hgvsp: ENSP00000265312.6:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2719G>A
  hgvsp: ENSP00000273049.7:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2719G>A
  hgvsp: ENSP00000410422.1:p.Val907Met
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val907Met
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

2-216271230-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271230
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271230
    reference: chr 2
allele count: 12
allele frequency: 1.037685270057592e-4
allele num: 115642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2717C>T
  hgvsp: ENSP00000323534.6:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2717C>T
  hgvsp: ENSP00000265312.6:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2717C>T
  hgvsp: ENSP00000410422.1:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2717C>T
  hgvsp: ENSP00000338200.4:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2717C>T
  hgvsp: ENSP00000399538.2:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2717C>T
  hgvsp: ENSP00000394423.1:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2717C>T
  hgvsp: ENSP00000415018.1:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2717C>T
  hgvsp: ENSP00000348285.4:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2717C>T
  hgvsp: ENSP00000346839.4:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2717C>T
  hgvsp: ENSP00000352696.1:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2717C>T
  hgvsp: ENSP00000349509.2:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2717C>T
  hgvsp: ENSP00000350534.4:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2717C>T
  hgvsp: ENSP00000273049.7:p.Thr906Ile
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22637
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15565
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr906Ile
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

2-216271240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271240
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271240
    reference: chr 2
allele count: 1
allele frequency: 8.780402142418123e-6
allele num: 113890
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2714-7C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.2714-7C>T
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/2-216271242-CAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271242
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271240
    reference: chr 2
allele count: 449
allele frequency: 3.957760383611875e-3
allele num: 113448
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2714-11_2714-10delTT
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13680
  bin: 2.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 1.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 9875
  bin: 1.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 19214
  bin: 2.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 3.25e1
  variant carriers: 25
genotype quality: GenotypeQuality
num of homozygotes: 7
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: CAA
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

2-216271243-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271243
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271243
    reference: chr 2
allele count: 1
allele frequency: 8.882414595583663e-6
allele num: 112582
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2714-10T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13708
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

2-216271246-A-ACCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271246
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271249
    reference: chr 2
allele count: 1
allele frequency: 8.868864962662078e-6
allele num: 112754
alternate allele: ACCT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2714-14_2714-13insAGG
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

2-216271248-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271248
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271248
    reference: chr 2
allele count: 1
allele frequency: 8.912338241060925e-6
allele num: 112204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2714-15A>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13086
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

2-216271251-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271251
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271251
    reference: chr 2
allele count: 1
allele frequency: 8.941024999105897e-6
allele num: 111844
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2714-18T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

2-216271253-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271253
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271253
    reference: chr 2
allele count: 1
allele frequency: 8.977950154420743e-6
allele num: 111384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2714-20A>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

2-216271277-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271277
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271277
    reference: chr 2
allele count: 2
allele frequency: 1.929347301807798e-5
allele num: 103662
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2714-44C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20514
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14904
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

2-216271277-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271277
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271277
    reference: chr 2
allele count: 1
allele frequency: 9.646736509038992e-6
allele num: 103662
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2714-44C>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14904
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

2-216271281-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271281
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271281
    reference: chr 2
allele count: 1
allele frequency: 1.000960922485586e-5
allele num: 99904
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2714-48T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14720
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6275
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

2-216271283-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271283
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271283
    reference: chr 2
allele count: 1
allele frequency: 1.001662760181902e-5
allele num: 99834
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2714-50A>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum

2-216271803-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271803
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271803
    reference: chr 2
allele count: 1
allele frequency: 8.265145879824779e-6
allele num: 120990
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2713+47T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9123
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

2-216271812-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271812
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271812
    reference: chr 2
allele count: 43293
allele frequency: 3.578998710360107e-1
allele num: 120964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2713+38T>A
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 2.75e1
  variant carriers: 1481
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 3.25e1
  variant carriers: 2639
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 5.75e1
  variant carriers: 2894
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 510
genotype depth: GenotypeDepth
  all individuals: 7781
  bin: 4.25e1
  variant carriers: 4374
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 5.25e1
  variant carriers: 3632
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 7.75e1
  variant carriers: 1038
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 8.75e1
  variant carriers: 742
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 6.75e1
  variant carriers: 1685
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 9.75e1
  variant carriers: 2688
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 8.25e1
  variant carriers: 802
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 2.25e1
  variant carriers: 635
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 3.75e1
  variant carriers: 3668
genotype quality: GenotypeQuality
num of homozygotes: 8513
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

2-216271812-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271812
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271812
    reference: chr 2
allele count: 1
allele frequency: 8.266922390132602e-6
allele num: 120964
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2713+38T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7781
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

2-216271813-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271813
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271813
    reference: chr 2
allele count: 8
allele frequency: 6.604256443277693e-5
allele num: 121134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2713+37A>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9006
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6741
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8680
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-216271816-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271816
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271816
    reference: chr 2
allele count: 2
allele frequency: 1.650982334489021e-5
allele num: 121140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2713+34C>A
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

2-216271818-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271818
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271818
    reference: chr 2
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2713+32A>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

2-216271829-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271829
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271829
    reference: chr 2
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2713+21C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6745
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-216271830-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271830
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271830
    reference: chr 2
allele count: 12
allele frequency: 9.8956014051754e-5
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2713+20A>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8773
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-216271831-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271831
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271831
    reference: chr 2
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2713+19C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5888
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

2-216271844-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271844
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271844
    reference: chr 2
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2713+6T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2713+6T>C
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-216271856-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271856
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271856
    reference: chr 2
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2707C>A
  hgvsp: ENSP00000352696.1:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2707C>A
  hgvsp: ENSP00000273049.7:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2707C>A
  hgvsp: ENSP00000265312.6:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2707C>A
  hgvsp: ENSP00000346839.4:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2707C>A
  hgvsp: ENSP00000350534.4:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2707C>A
  hgvsp: ENSP00000348285.4:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2707C>A
  hgvsp: ENSP00000349509.2:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2707C>A
  hgvsp: ENSP00000415018.1:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2707C>A
  hgvsp: ENSP00000394423.1:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2707C>A
  hgvsp: ENSP00000410422.1:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2707C>A
  hgvsp: ENSP00000399538.2:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2707C>A
  hgvsp: ENSP00000323534.6:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2707C>A
  hgvsp: ENSP00000338200.4:p.Arg903Ser
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg903Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

2-216271860-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271860
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271860
    reference: chr 2
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2703C>T
  hgvsp: ENST00000446046.1:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2703C>T
  hgvsp: ENST00000421182.1:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2703C>T
  hgvsp: ENST00000354785.4:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2703C>T
  hgvsp: ENST00000336916.4:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2703C>T
  hgvsp: ENST00000432072.2:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2703C>T
  hgvsp: ENST00000345488.5:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2703C>T
  hgvsp: ENST00000346544.3:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2703C>T
  hgvsp: ENST00000359671.1:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2703C>T
  hgvsp: ENST00000356005.4:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2703C>T
  hgvsp: ENST00000357009.2:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2703C>T
  hgvsp: ENST00000443816.1:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2703C>T
  hgvsp: ENST00000357867.4:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2703C>T
  hgvsp: ENST00000323926.6:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr901Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

2-216271861-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271861
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271861
    reference: chr 2
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2702C>T
  hgvsp: ENSP00000352696.1:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2702C>T
  hgvsp: ENSP00000394423.1:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2702C>T
  hgvsp: ENSP00000265312.6:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2702C>T
  hgvsp: ENSP00000273049.7:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2702C>T
  hgvsp: ENSP00000349509.2:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2702C>T
  hgvsp: ENSP00000346839.4:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2702C>T
  hgvsp: ENSP00000415018.1:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2702C>T
  hgvsp: ENSP00000338200.4:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2702C>T
  hgvsp: ENSP00000348285.4:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2702C>T
  hgvsp: ENSP00000350534.4:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2702C>T
  hgvsp: ENSP00000399538.2:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2702C>T
  hgvsp: ENSP00000410422.1:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2702C>T
  hgvsp: ENSP00000323534.6:p.Thr901Ile
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr901Ile
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

2-216271861-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271861
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271861
    reference: chr 2
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2702C>A
  hgvsp: ENSP00000394423.1:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2702C>A
  hgvsp: ENSP00000415018.1:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2702C>A
  hgvsp: ENSP00000348285.4:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2702C>A
  hgvsp: ENSP00000346839.4:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2702C>A
  hgvsp: ENSP00000323534.6:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2702C>A
  hgvsp: ENSP00000338200.4:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2702C>A
  hgvsp: ENSP00000273049.7:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2702C>A
  hgvsp: ENSP00000352696.1:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2702C>A
  hgvsp: ENSP00000410422.1:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2702C>A
  hgvsp: ENSP00000349509.2:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2702C>A
  hgvsp: ENSP00000265312.6:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2702C>A
  hgvsp: ENSP00000399538.2:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2702C>A
  hgvsp: ENSP00000350534.4:p.Thr901Asn
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr901Asn
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

2-216271870-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271870
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271870
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2693C>T
  hgvsp: ENSP00000410422.1:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2693C>T
  hgvsp: ENSP00000352696.1:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2693C>T
  hgvsp: ENSP00000348285.4:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2693C>T
  hgvsp: ENSP00000415018.1:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2693C>T
  hgvsp: ENSP00000265312.6:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2693C>T
  hgvsp: ENSP00000394423.1:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2693C>T
  hgvsp: ENSP00000338200.4:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2693C>T
  hgvsp: ENSP00000350534.4:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2693C>T
  hgvsp: ENSP00000399538.2:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2693C>T
  hgvsp: ENSP00000273049.7:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2693C>T
  hgvsp: ENSP00000346839.4:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2693C>T
  hgvsp: ENSP00000349509.2:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2693C>T
  hgvsp: ENSP00000323534.6:p.Thr898Ile
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr898Ile
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

2-216271878-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271878
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271878
    reference: chr 2
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2685A>G
  hgvsp: ENST00000323926.6:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2685A>G
  hgvsp: ENST00000359671.1:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2685A>G
  hgvsp: ENST00000354785.4:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2685A>G
  hgvsp: ENST00000357867.4:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2685A>G
  hgvsp: ENST00000432072.2:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2685A>G
  hgvsp: ENST00000345488.5:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2685A>G
  hgvsp: ENST00000446046.1:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2685A>G
  hgvsp: ENST00000421182.1:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2685A>G
  hgvsp: ENST00000443816.1:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2685A>G
  hgvsp: ENST00000356005.4:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2685A>G
  hgvsp: ENST00000357009.2:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2685A>G
  hgvsp: ENST00000336916.4:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2685A>G
  hgvsp: ENST00000346544.3:c.2685A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln895Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD

2-216271889-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216271889
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216271889
    reference: chr 2
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.2674G>A
  hgvsp: ENSP00000273049.7:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.2674G>A
  hgvsp: ENSP00000346839.4:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.2674G>A
  hgvsp: ENSP00000399538.2:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.2674G>A
  hgvsp: ENSP00000415018.1:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.2674G>A
  hgvsp: ENSP00000394423.1:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.2674G>A
  hgvsp: ENSP00000338200.4:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.2674G>A
  hgvsp: ENSP00000350534.4:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.2674G>A
  hgvsp: ENSP00000352696.1:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.2674G>A
  hgvsp: ENSP00000265312.6:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.2674G>A
  hgvsp: ENSP00000349509.2:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.2674G>A
  hgvsp: ENSP00000348285.4:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.2674G>A
  hgvsp: ENSP00000323534.6:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.2674G>A
  hgvsp: ENSP00000410422.1:p.Val892Ile
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8789
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val892Ile
num of homozygotes: 0
population: Latino
reference allele: C

GenotypeDepth
all individuals: 571
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 755
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14178
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1768
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 97
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40056
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5855
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 97
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2256
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1133
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2305
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7748
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 1.840403e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.224e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: 6.57e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

QD
type: SiteQuality
SIO_000300: 1.304e1

GenotypeDepth
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 740
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 799
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 756
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40065
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5853
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2247
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7746
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.51e-1

DP
type: SiteQuality
SIO_000300: 1.839843e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

FS
type: SiteQuality
SIO_000300: 1.145e0

MQRankSum
type: SiteQuality
SIO_000300: -1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.532e-1

QD
type: SiteQuality
SIO_000300: 1.425e1

GenotypeDepth
all individuals: 8770
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1767
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 755
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7739
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5848
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 465
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40077
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2300
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 9.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.6e-2

DP
type: SiteQuality
SIO_000300: 1.839867e6

MQ
type: SiteQuality
SIO_000300: 5.928e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.33e-1

FS
type: SiteQuality
SIO_000300: 1.016e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.133e0

VQSLOD
type: SiteQuality
SIO_000300: -6.48e-2

GenotypeDepth
all individuals: 798
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 407
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14279
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 743
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7683
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5834
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 58
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40076
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2278
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2206
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-2

DP
type: SiteQuality
SIO_000300: 1.838235e6

QD
type: SiteQuality
SIO_000300: 1.405e1

GenotypeDepth
all individuals: 101
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14292
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 798
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 741
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 572
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1117
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 413
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7685
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40081
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5836
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 2279
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 9
allele frequency: 8.660508083140878e-4
allele num: 10392
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: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

FS
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.933e1

DP
type: SiteQuality
SIO_000300: 1.8377e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

QD
type: SiteQuality
SIO_000300: 1.318e1

GenotypeDepth
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29285
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 407
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 571
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1709
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8715
bin: 3.25e1
variant carriers: 0

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

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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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African
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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QD
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MQ
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

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

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

European (Non-Finnish)
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African
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East Asian
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Other
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South Asian
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European (Finnish)
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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FS
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ClippingRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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African
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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DP
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GenotypeDepth
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South Asian
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Latino
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East Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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MQRankSum
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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MQ
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ClippingRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
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

Latino
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allele count: 0
allele frequency: 0.0e0
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Other
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: -5.34e-1

DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.507076109491902e-5
allele num: 66562
num of homozygotes: 0

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

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

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

Other
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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MQ
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BaseQRankSum
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QD
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66562
num of homozygotes: 0

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

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

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

African
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allele count: 0
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Latino
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European (Finnish)
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South Asian
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East Asian
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Other
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QD
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FS
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InbreedingCoeff
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MQ
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DP
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.005259203606311e-5
allele num: 66550
num of homozygotes: 0

European (Finnish)
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Latino
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South Asian
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East Asian
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allele num: 8614
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Other
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African
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ReadPosRankSum
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InbreedingCoeff
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FS
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QD
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MQ
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VQSLOD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
type: Population
allele count: 0
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num of homozygotes: 0

Latino
type: Population
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allele frequency: 3.006524157421605e-5
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European (Finnish)
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African
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East Asian
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Other
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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QD
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MQ
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InbreedingCoeff
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DP
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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South Asian
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Other
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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QD
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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Other
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ReadPosRankSum
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VQSLOD
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MQ
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FS
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 1.16504854368932e-3
allele num: 10300
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.513912859175826e-5
allele num: 66054
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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South Asian
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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FS
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MQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.517220452131695e-5
allele num: 65910
num of homozygotes: 0

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

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

European (Finnish)
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African
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Latino
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East Asian
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South Asian
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Other
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DP
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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FS
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QD
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MQ
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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African
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European (Finnish)
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQ
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MQRankSum
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QD
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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Other
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African
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European (Non-Finnish)
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Latino
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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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ClippingRankSum
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ReadPosRankSum
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DP
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.726248391450362e-4
allele num: 63722
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Latino
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African
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East Asian
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QD
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ClippingRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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East Asian
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African
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South Asian
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European (Non-Finnish)
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MQ
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FS
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MQRankSum
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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Other
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African
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European (Finnish)
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DP
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QD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.628558400104228e-5
allele num: 61404
num of homozygotes: 0

Other
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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MQRankSum
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MQ
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DP
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.2e-3

QD
type: SiteQuality
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
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allele count: 2
allele frequency: 3.497481813094572e-5
allele num: 57184
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

African
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num of homozygotes: 0

Latino
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Other
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East Asian
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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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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SIO_000300: -2.93e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8808
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57184
num of homozygotes: 0

South Asian
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allele num: 14508
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.35e-1

MQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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SIO_000300: 1.204533e6

MQ
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SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14190
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 55112
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5422
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.096731739416539e-4
allele num: 9118
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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DP
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MQ
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SIO_000300: 5.884e1

VQSLOD
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ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: -2.28e-1

InbreedingCoeff
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SIO_000300: -4.6e-3

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6774
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 1.174536058256989e-4
allele num: 8514
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 55018
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14200
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: -3.7e-2

QD
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VQSLOD
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MQ
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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FS
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ClippingRankSum
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SIO_000300: -4.1e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 9.881422924901186e-5
allele num: 10120
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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 frequency: 0.0e0
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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)
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allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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FS
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QD
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 2167

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 13

East Asian
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allele count: 610
allele frequency: 7.063455303381196e-2
allele num: 8636
num of homozygotes: 19

African
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allele count: 2081
allele frequency: 2.043000196347929e-1
allele num: 10186
num of homozygotes: 224

Latino
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allele count: 3237
allele frequency: 2.805998613037448e-1
allele num: 11536
num of homozygotes: 458

South Asian
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allele count: 8144
allele frequency: 4.932170542635659e-1
allele num: 16512
num of homozygotes: 2021

European (Non-Finnish)
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allele count: 26365
allele frequency: 3.959778919227419e-1
allele num: 66582
num of homozygotes: 5251

Other
type: Population
allele count: 315
allele frequency: 3.469162995594713e-1
allele num: 908
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European (Finnish)
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allele count: 2541
allele frequency: 3.847668079951544e-1
allele num: 6604
num of homozygotes: 486

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

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

South Asian
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num of homozygotes: 0

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

African
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num of homozygotes: 0

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

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

South Asian
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Latino
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European (Non-Finnish)
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allele num: 66740
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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European (Non-Finnish)
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Latino
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allele num: 11578
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.229e0

VQSLOD
type: SiteQuality
SIO_000300: 2.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.856222e6

MQ
type: SiteQuality
SIO_000300: 5.988e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.53e0

FS
type: SiteQuality
SIO_000300: 4.142e0

QD
type: SiteQuality
SIO_000300: 1.581e1

GenotypeDepth
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8338
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 680
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 500
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4879
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6247
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3735
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3877
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2439
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4103
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 33992
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4131
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0